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Gabapentin Can be Used for Restless Legs Syndrome

What is restless legs syndrome?

Restless legs syndrome (RLS), also called Willis-Ekbom Disease, causes unpleasant or uncomfortable sensations in the legs and an irresistible urge to move them.  Symptoms commonly occur in the late afternoon or evening hours, and are often most severe at night when a person is resting, such as sitting or lying in bed.

Restless Legs Syndrome Fact Sheet
Restless Legs Syndrome Fact Sheet

They also may occur when someone is inactive and sitting for extended periods (for example, when taking a trip by plane or watching a movie).  Since symptoms can increase in severity during the night, it could become difficult to fall asleep or return to sleep after waking up.  Moving the legs or walking typically relieves the discomfort but the sensations often recur once the movement stops.  RLS is classified as a sleep disorder since the symptoms are triggered by resting and attempting to sleep, and as a movement disorder, since people are forced to move their legs in order to relieve symptoms.  It is, however, best characterized as a neurological sensory disorder with symptoms that are produced from within the brain itself.

RLS is one of several disorders that can cause exhaustion and daytime sleepiness, which can strongly affect mood, concentration, job and school performance, and personal relationships.  Many people with RLS report they are often unable to concentrate, have impaired memory, or fail to accomplish daily tasks.  Untreated moderate to severe RLS can lead to about a 20 percent decrease in work productivity and can contribute to depression and anxiety.  It also can make traveling difficult.

It is estimated that up to 7-10 percent of the U.S. population may have RLS.  RLS occurs in both men and women, although women are more likely to have it than men.   It may begin at any age.  Many individuals who are severely affected are middle-aged or older, and the symptoms typically become more frequent and last longer with age.

More than 80 percent of people with RLS also experience periodic limb movement of sleep (PLMS).  PLMS is characterized by involuntary leg (and sometimes arm) twitching or jerking movements during sleep that typically occur every 15 to 40 seconds, sometimes throughout the night.  Although many individuals with RLS also develop PLMS, most people with PLMS do not experience RLS.

Fortunately, most cases of RLS can be treated with non-drug therapies and if necessary, medications.

What are common signs and symptoms of restless legs?

People with RLS feel the irresistible urge to move, which is accompanied by uncomfortable sensations in their lower limbs that are unlike normal sensations experienced by people without the disorder.  The sensations in their legs are often difficult to define but may be described as aching throbbing, pulling, itching, crawling, or creeping.  These sensations less commonly affect the arms, and rarely the chest or head.  Although the sensations can occur on just one side of the body, they most often affect both sides.  They can also alternate between sides. The sensations range in severity from uncomfortable to irritating to painful.

Because moving the legs (or other affected parts of the body) relieves the discomfort, people with RLS often keep their legs in motion to minimize or prevent the sensations.  They may pace the floor, constantly move their legs while sitting, and toss and turn in bed.

A classic feature of RLS is that the symptoms are worse at night with a distinct symptom-free period in the early morning, allowing for more refreshing sleep at that time.  Some people with RLS have difficulty falling asleep and staying asleep.  They may also note a worsening of symptoms if their sleep is further reduced by events or activity.

RLS symptoms may vary from day to day, in severity and frequency, and from person to person.  In moderately severe cases, symptoms occur only once or twice a week but often result in significant delay of sleep onset, with some disruption of daytime function.  In severe cases of RLS, the symptoms occur more than twice a week and result in burdensome interruption of sleep and impairment of daytime function.

People with RLS can sometimes experience remissions—spontaneous improvement over a period of weeks or months before symptoms reappear—usually during the early stages of the disorder.  In general, however, symptoms become more severe over time.

People who have both RLS and an associated medical condition tend to develop more severe symptoms rapidly.  In contrast, those who have RLS that is not related to any other condition show a very slow progression of the disorder, particularly if they experience onset at an early age; many years may pass before symptoms occur regularly.

What causes restless legs syndrome?

In most cases, the cause of RLS is unknown (called primary RLS).  However, RLS has a genetic component and can be found in families where the onset of symptoms is before age 40.  Specific gene variants have been associated with RLS.  Evidence indicates that low levels of iron in the brain also may be responsible for RLS.

Considerable evidence also suggests that RLS is related to a dysfunction in one of the sections of the brain that control movement (called the basal ganglia) that use the brain chemical dopamine.  Dopamine is needed to produce smooth, purposeful muscle activity and movement.  Disruption of these pathways frequently results in involuntary movements.  Individuals with Parkinson’s disease, another disorder of the basal ganglia’s dopamine pathways, have increased chance of developing RLS.

RLS also appears to be related to or accompany the following factors or underlying conditions:

  • end-stage renal disease and hemodialysis
  • iron deficiency
  • certain medications that may aggravate RLS symptoms, such as antinausea drugs (e.g. prochlorperazine or metoclopramide), antipsychotic drugs (e.g., haloperidol or phenothiazine derivatives), antidepressants that increase serotonin (e.g., fluoxetine or sertraline), and some cold and allergy medications that contain older antihistamines (e.g., diphenhydramine)
  • use of alcohol, nicotine, and caffeine
  • pregnancy, especially in the last trimester; in most cases, symptoms usually disappear within 4 weeks after delivery
  • neuropathy (nerve damage).

Sleep deprivation and other sleep conditions like sleep apnea also may aggravate or trigger symptoms in some people.  Reducing or completely eliminating these factors may relieve symptoms.

How is restless legs syndrome diagnosed?

Since there is no specific test for RLS, the condition is diagnosed by a doctor’s evaluation.  The five basic criteria for clinically diagnosing the disorder are:

  • A strong and often overwhelming need or urge to move the legs that is often associated with abnormal, unpleasant, or uncomfortable sensations.
  • The urge to move the legs starts or get worse during rest or inactivity.
  • The urge to move the legs is at least temporarily and partially or totally relieved by movements.
  • The urge to move the legs starts or is aggravated in the evening or night.
  • The above four features are not due to any other medical or behavioral condition.

A physician will focus largely on the individual’s descriptions of symptoms, their triggers and relieving factors, as well as the presence or absence of symptoms throughout the day.  A neurological and physical exam, plus information from the person’s medical and family history and list of current medications, may be helpful.  Individuals may be asked about frequency, duration, and intensity of symptoms; if movement helps to relieve symptoms; how much time it takes to fall asleep; any pain related to symptoms; and any tendency toward daytime sleep patterns and sleepiness, disturbance of sleep, or daytime function.  Laboratory tests may rule out other conditions such as kidney failure, iron deficiency anemia (which is a separate condition related to iron deficiency), or pregnancy that may be causing symptoms of RLS.  Blood tests can identify iron deficiencies as well as other medical disorders associated with RLS.  In some cases, sleep studies such as polysomnography (a test that records the individual’s brain waves, heartbeat, breathing, and leg movements during an entire night) may identify the presence of other causes of sleep disruption (e.g., sleep apnea), which may impact management of the disorder.  Periodic limb movement of sleep during a sleep study can support the diagnosis of RLS but, again, is not exclusively seen in individuals with RLS.

Diagnosing RLS in children may be especially difficult, since it may be hard for children to describe what they are experiencing, when and how often the symptoms occur, and how long symptoms last.  Pediatric RLS can sometimes be misdiagnosed as “growing pains” or attention deficit disorder.

How is restless legs syndrome treated?

RLS can be treated, with care directed toward relieving symptoms.  Moving the affected limb(s) may provide temporary relief.  Sometimes RLS symptoms can be controlled by finding and treating an associated medical condition, such as peripheral neuropathy, diabetes, or iron deficiency anemia.

Iron supplementation or medications are usually helpful but no single medication effectively manages RLS for all individuals.  Trials of different drugs may be necessary.  In addition, medications taken regularly may lose their effect over time or even make the condition worse, making it necessary to change medications.

Treatment options for RLS include:

 Lifestyle changes Certain lifestyle changes and activities may provide some relief in persons with mild to moderate symptoms of RLS.  These steps include avoiding or decreasing the use of alcohol and tobacco, changing or maintaining a regular sleep pattern, a program of moderate exercise, and massaging the legs, taking a warm bath, or using a heating pad or ice pack.  There are new medical devices that have been cleared by the U.S. Food & Drug Administration (FDA), including a foot wrap that puts pressure underneath the foot and another that is a pad that delivers vibration to the back of the legs.  Aerobic and leg-stretching exercises of moderate intensity also may provide some relief from mild symptoms.

Iron.  For individuals with low or low-normal blood tests called ferritin and transferrin saturation, a trial of iron supplements is recommended as the first treatment.  Iron supplements are available over-the-counter.  A common side effect is upset stomach, which may improve with use of a different type of iron supplement.  Because iron is not well-absorbed into the body by the gut, it may cause constipation that can be treated with a stool softeners such as polyethylene glycol.  In some people, iron supplementation does not improve a person’s iron levels.  Others may require iron given through an IV line in order to boost the iron levels and relieve symptoms.

Anti-seizure drugs Anti-seizure drugs are becoming the first-line prescription drugs for those with RLS.  The FDA has approved gabapentin enacarbil for the treatment of moderate to severe RLS, This drug appears to be as effective as dopaminergic treatment (discussed below) and, at least to date, there have been no reports of problems with a progressive worsening of symptoms due to medication (called augmentation).  Other medications may be prescribed “off-label” to relieve some of the symptoms of the disorder.

Other anti-seizure drugs such as the standard form of gabapentin and pregabalin can decrease such sensory disturbances as creeping and crawling as well as nerve pain.  Dizziness, fatigue, and sleepiness are among the possible side effects.  Recent studies have shown that pregabalin is as effective for RLS treatment as the dopaminergic drug pramipexole, suggesting this class of drug offers equivalent benefits.

Dopaminergic agents These drugs, which increase dopamine effect, are largely used to treat Parkinson’s disease.  They have been shown to reduce symptoms of RLS when they are taken at nighttime.  The FDA has approved ropinirole, pramipexole, and rotigotine to treat moderate to severe RLS.  These drugs are generally well tolerated but can cause nausea, dizziness, or other short-term side effects.  Levodopa plus carbidopa may be effective when used intermittently, but not daily.

Although dopamine-related medications are effective in managing RLS symptoms, long-term use can lead to worsening of the symptoms in many individuals.  With chronic use, a person may begin to experience symptoms earlier in the evening or even earlier until the symptoms are present around the clock.  Over time, the initial evening or bedtime dose can become less effective, the symptoms at night become more intense, and symptoms could begin to affect the arms or trunk.  Fortunately, this apparent progression can be reversed by removing the person from all dopamine-related medications.

Another important adverse effect of dopamine medications that occurs in some people is the development of impulsive or obsessive behaviors such as obsessive gambling or shopping.  Should they occur, these behaviors can be improved or reversed by stopping the medication.

Opioids.  Drugs such as methadone, codeine, hydrocodone, or oxycodone are sometimes prescribed to treat individuals with more severe symptoms of RLS who did not respond well to other medications.  Side effects include constipation, dizziness, nausea, exacerbation of sleep apnea, and the risk of addiction; however, very low doses are often effective in controlling symptoms of RLS.

Benzodiazepines.  These drugs can help individuals obtain a more restful sleep.  However, even if taken only at bedtime they can sometimes cause daytime sleepiness, reduce energy, and affect concentration.  Benzodiazepines such as clonazepam and lorazepam are generally prescribed to treat anxiety, muscle spasms, and insomnia.  Because these drugs also may induce or aggravate sleep apnea in some cases, they should not be used in people with this condition.  These are last-line drugs due to their side effects.

What is the prognosis for people with restless legs syndrome?

RLS is generally a lifelong condition for which there is no cure.  However, current therapies can control the disorder, minimize symptoms, and increase periods of restful sleep.  Symptoms may gradually worsen with age, although the decline may be somewhat faster for individuals who also suffer from an associated medical condition.  A diagnosis of RLS does not indicate the onset of another neurological disease, such as Parkinson’s disease.  In addition, some individuals have remissions—periods in which symptoms decrease or disappear for days, weeks, months, or years—although symptoms often eventually reappear.  If RLS symptoms are mild, do not produce significant daytime discomfort, or do not affect an individual’s ability to fall asleep, the condition does not have to be treated.

What research is being done?

The mission of the National Institute of Neurological Disorders and Stroke is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.  The NINDS is a component of the National Institutes of Health , the leading supporter of biomedical research in the world.

While the direct cause of RLS is often unknown, changes in the brain’s signaling pathways are likely to contribute to the disease.  In particular, researchers suspect that impaired transmission of dopamine signals in the brain’s basal ganglia may play a role.  There is a relationship between genetics and RLS.  However, currently there is no genetic testing.  NINDS-supported research is ongoing to help discover genetic relationships and to better understand what causes the disease.

The NINDS also supports research on why the use of dopamine agents to treat RLS, Parkinson’s disease, and other movement disorders can lead to impulse control disorders, with aims to develop new or improved treatments that avoid this adverse effect.

The brain arousal systems appear to be overactive in RLS and may produce both the need to move when trying to rest and the inability to maintain sleep.  NINDS-funded researchers are using advanced magnetic resonance imaging (MRI) to measure brain chemical changes in individuals with RLS and evaluate their relation to the disorder’s symptoms in hopes of developing new research models and ways to correct the overactive arousal process.  Since scientists currently don’t fully understand the mechanisms by which iron gets into the brain and how those mechanisms are regulated, NINDS-funded researchers are studying the role of endothelial cells—part of the protective lining called the blood-brain barrier that separates circulating blood from the fluid surrounding brain tissue—in the regulation of cerebral iron metabolism.  Results may offer new insights to treating the cognitive and movement symptoms associated with these disorders.

More information about research on RLS supported by NINDS or other components of the NIH is available through the NIH RePORTER (http://projectreporter.nih.gov/reporter.cfm), a searchable database of current and previously funded research, as well as research results such as publications.

What is Fioricet and What is the Benefits of Fioricet ?

Fioricet contains a combination of acetaminophen, butalbital, and caffeine. Acetaminophen is a pain reliever and fever reducer.

Butalbital is in a group of drugs called barbiturates. It relaxes muscle contractions involved in a tension headache.

Caffeine is a central nervous system stimulant. It relaxes muscle contractions in blood vessels to improve blood flow.

Fioricet is used to treat tension headaches that are caused by muscle contractions.

Fioricet® (Butalbital, Acetaminophen, and Caffeine Tablets USP) is supplied in tablet form for oral administration.

Each tablet contains the following active ingredients:
butalbital USP . . . . . . . . . . . .50 mg
acetaminophen USP . . . . . . 325 mg
caffeine USP . . . . . . . . . . . . .40 mg

Inactive Ingredients: crospovidone, FD&C Blue #1, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, and stearic acid.

Butalbital (5-allyl-5-isobutylbarbituric acid), is a short to intermediate-acting barbiturate. It has the following structural formula:

 

Butalbital structural formula illustration

 

C11H16N2O3          Mol. wt. 224.26

Acetaminophen (4´-hydroxyacetanilide), is a non-opiate, non-salicylateanalgesic and antipyretic. It has the following structural formula:

 

Acetaminophen structural formula illustration

 

C8H9NO2              Mol. wt. 151.17

Caffeine (1,3,7-trimethylxanthine), is a central nervous system stimulant. It has the following structural formula:

 

Caffeine structural formula illustration

 

C8H10N4O2          Mol. wt. 194.19

Fioricet can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Avoid drinking alcohol. It may increase your risk of liver damage while taking acetaminophen.

Ask a doctor or pharmacist before using any other cold, allergy, pain, or sleep medication. Acetaminophen (sometimes abbreviated as APAP) is contained in many combination medicines. Taking certain products together can cause you to get too much acetaminophen which can lead to a fatal overdose. Check the label to see if a medicine contains acetaminophen or APAP.

While you are taking Fioricet, avoid taking diet pills, caffeine pills, or other stimulants (such as ADHD medications) without your doctor’s advice.

Fioricet (butalbital, acetaminophen and caffeine) ® (Butalbital,Acetaminophen, and Caffeine Tablets USP) is indicated for the relief of the symptom complex of tension (or muscle contraction) headache.

Evidence supporting the efficacy and safety of this combination product in the treatment of multiple recurrent headaches is unavailable. Caution in this regard is required because butalbital is habit-forming and potentially abusable.

Why is Fioricet used to treat migraine?

Fioricet is an older medication that used to frequently be prescribed to treat migraine symptoms. However, there is not enough evidence that shows it’s effective for migraine attacks, especially when compared to safer products.

Although Fioricet has been used for many years for migraine, it’s not approved for this use, and there are greater risks  than benefits with this medication.

Fioricet may be an option if other migraine treatment options have not worked. Your doctor will just want to monitor you closely to avoid side effects.

It’s prescribed to help relieve immediate headache symptoms, but not to prevent migraine attacks.

How does Fioricet work?

The acetaminophen in Fioricet is a pain reliever, the caffeine works as a stimulant to increase the acetaminophen’s effectiveness, and the butalbital is a sedative that decreases anxiety while causing relaxation and sleepiness. These actions are believed to ease migraine symptoms, but there is limited evidence that barbituates ease migraine symptoms.

What are the possible side effects of Fioricet?

The most common side effects from Fioricet include:

  • Drowsiness
  • Upset stomach
  • Vomiting
  • Stomach pain
  • Depression
  • Lightheadedness
  • Confusion

The following side effects could be signs of allergy or more serious complications and should be reported to health provider immediately:

  • Skin rash
  • Itching
  • Difficulty breathing

This is not an exhaustive list of all potential side effects of Fioricet. For more information, consult your doctor or healthcare provider. Patients should talk to their doctor about what to expect with treatment with Fioricet. If you notice any new or worsening side effects, contact your doctor or healthcare provider immediately.

Things to note about Fioricet

Fioricet can be habit-forming, so you should use extreme caution if you decide to take it. Additionally, some people who take barbituates or opioids for extended periods can experience rebound headaches, which can increase in severity. These are also known as MOH, or medication overuse headaches.1

Barbituates can cause drowsiness, and their effect can be increased by alcohol use. It is important not to drive or use heavy machinery until you know how this drug affects you.2

Before taking Fioricet, tell your doctor if you:

  • Are allergic to any ingredients in the medication
  • Are taking blood thinners, antidepressants, antihistamines, or other sedatives like sleeping pills or tranquilizers.
  • Are taking pain medications. Many over-the-counter pain relievers contain acetaminophen, and too much of this drug can be harmful.
  • Have ever had liver disease, porphyria, or depression
  • Are pregnant, plan to become pregnant, or are breastfeeding2

You should begin no medication or supplement without first checking with your health care provider and should let them know of any other prescriptions, OTCs, and herbals you are taking to ensure there are no interactions.

What is the most important information I should know about Fioricet (Acetaminophen, Butalbital, And Caffeine)?

Do not use this medicine if you have taken an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, phenelzine, rasagiline, selegiline, and tranylcypromine.

You should not use acetaminophen, butalbital, and caffeine if you are allergic to it, if you have porphyria, or if you have recently used alcohol, sedatives, tranquilizers, or other narcotic medications.

To make sure acetaminophen, butalbital, and caffeine is safe for you, tell your doctor if you have:

  • liver disease, cirrhosis, a history of alcoholism or drug addiction, or if you drink more than 3 alcoholic beverages per day;
  • kidney disease;
  • asthma, sleep apnea, or other breathing disorder;
  • stomach ulcer or bleeding;
  • a history of skin rash caused by any medication;
  • a history of mental illness or suicidal thoughts; or
  • if you use medicine to prevent blood clots.

It is not known whether this medicine will harm an unborn baby. If you use butalbital while you are pregnant, your baby could become dependent on the drug. This can cause life-threatening withdrawal symptoms in the baby after it is born. Babies born dependent on habit-forming medicine may need medical treatment for several weeks. Tell your doctor if you are pregnant or plan to become pregnant.

This medicine can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Why is fioricet exempt ? Exempt Prescription Products List (2)

Exempt Prescription Products

2/21/2020

Company Trade Name NDC Code Form Controlled Substance

(mg or mg/ml)

Mikart, Inc. Tencon (Butalbital and Acetaminophen 50mg/325mg) 11584-0030 TB Butalbital

50.00

Mikart, Inc./Shionogi, Inc. Dolgic Plus Tablets 59630-074 TB Butalbital

50.00

Moore Medical Corporation Antispasmodic Tabs 00839-5055 TB Phenobarbtal

16.20

Moore Medical Corporation Butalbital, Acetaminophen and Caffeine Tablets 00839-7831 TB Butalbital

50.00

Morton Grove Pharmaceuticals, Inc. Antispasmodic Elixir 60432-0009 EL Phenobarbital

3.24

Nejo Pharmaceutical Spasmalones 00653-0002 TB Phenobarbital

16.00

Nexgen Pharma BUPAP (Butalbital and Acetaminophen 50mg/300mg) 0095-3000 TB Butalbital

50.00

Nexgen Pharma Butalbital with Acetaminophen and Caffeine Tablets 0722-7029 TB Butalbital

50.00

Nexgen Pharma Butalbital, Acetaminophen and Caffeine Tablets(50mg/325mg/40mg) 0722-7320 TB Butalbital

50.00

Northampton Medical, Inc. FEMCET 58436-0703 TB Butalbital

50.00

Oceanside Pharmaceuticals (Manufactured by Nexgen) Butalbital and Acetaminophen Tablets (50mg/300mg) 68682-306 TB Butalbital

50.00

Parke-Davis & Co Dilantin with Phenobarbital 1/2 00071-0531 CA Phenobarbital

32.00

Parke-Davis & Co Dilantin with Phenobarbital 1/4 00071-0375 CA Phenobarbital

16.00

Parke-Davis & Co Tedral SA 00071-0231 XT Phenobarbital

25.00

Parmed Pharmaceutical Sedapar Elixir 00349-4100 EL Phenobarbital

3.24

Parmed Pharmaceutical Sedapar Tablets 00349-2355 TB Phenobarbital

16.20

Pasadena Research Seds 00418-4072 TB Phenobarbital

16.20

PD-Rx Pharmaceuticals, Inc. Butalbital/APAP/Caffeine Tablets (50mg/325mg/40mg) 55289-0879 TB Butalbital

50.00

PD-Rx Pharmaceuticals, Inc. Donnatal Tablets 43063-601 TB Phenobarbital

16.20

Pecos Pharmaceuticals Phenobel Extentabs 59879-0110 TB Phenobarbital USP

48.60

Pernix Therapeutics Chlordiazepoxide HCL/ Clidinium Bromide Capsules 44183-0401 CA Chlordiazepoxide HCl

5.00

Pharmaceutical Basics Inc Butalbital, Acetaminophen and Caffeine Tablets 00832-1102 TB Butalbital

50.00

Pharmaceutical Basics Inc Clinibrax Capsules 00832-1054 CA Chlordiazepoxide HCl

5.00

PharmaTech LLC (Manufactured for Virtus Pharmaceutical) Chlordiazepoxide HCL and Clidinium Bromide Capsules 76439-302 CA Chlordiazepoxide HCl

5.00

Phlight Pharma, LLC. Allzital (Butalbital and Acetaminophen Tablets (25 mg/325 mg)) 70569-150 TB Butalbital

25.00

Pioneer Pharmaceuticals, Inc. Chlordiazepoxide HCL/ Clidinium Bromide Capsules 60104-4009 CA Chlordiazepoxide HCl

5.00

Poly Pharmaceuticals, Inc. Alagesic 50991-0302 CA Butalbital

50.00

Poythress & Co Inc Antrocol 00095-0041 CA Phenobarbital

16.00

Poythress & Co Inc Antrocol Elixir 00095-0042 EL Phenobarbital

3.00

Poythress & Co Inc Antrocol Tablets 00095-0040 TB Phenobarbital

16.00

Poythress & Co Inc Mudrane 00095-0050 TB Phenobarbital

8.00

Poythress & Co Inc Mudrane GG Elixir 00095-0053 EL Phenobarbital

0.50

Poythress & Co Inc Mudrane GG Tablets 00095-0051 TB Phenobarbital

8.00

Prasco Laboratories Phenobarbital, Hyoscyamine, Atropine, Scopolamine Tablets 66993-117 TB Phenobarbital

16.20

Prasco Laboratories Phenobarbital, Hyoscyamine, Atropine, Scopolamine Elixir (Grape) 66993-118 EL Phenobarbital

16.20

Prasco Laboratories Phenobarbital, Hyoscyamine, Atropine, Scopolamine Elixir (Mint) 66993-119 EL Phenobarbital

16.20

Private Formula Inc Sangesic 00511-1627 TB Butalbital

30.00

Qualitest Pharmaceuticals, Inc. Butalbital and Acetaminophen Tablets 0603-2540 TB Butalbital

50.00

Qualitest Pharmaceuticals, Inc. Butalbital, Acetaminophen and Caffeine Tablets 50/325/40mg 0603-2544 TB Butalbital

50.00

Qualitest Pharmaceuticals, Inc. Butalbital, Acetaminophen and Caffeine Tablets USP 0603-2547 TB Butalbital

50.00

8

Exempt Prescription Products

2/21/2020

Company Trade Name NDC Code Form Controlled Substance

(mg or mg/ml)

Qualitest Pharmaceuticals, Inc. Butalbital, Acetaminophen and Caffeine Tablets, USP 0603-2551 TB Butalbital

50.00

Qualitest Pharmaceuticals, Inc. Chlordiazepoxide Hydrochloride and Clidinium Bromide Capsules 0603-2714 CA Chlordiazepoxide

5.00

Qualitest Products Inc Butalbital, Acetaminophen and Caffeine Tablets 52446-0544 TB Butalbital

50.00

Qualitest Products Inc Chlordiazepoxide HCl 5 mg and Clidinium Br 2.5 mg 52446-0096 CA Chlordiazepoxide HCl

5.00

Redi-Med Butalbital Compound Capsules 53506-0103 CA Butalbital

50.00

Richlyn Laboratories Aminophylline & Phenobarbital 00115-2156 ET Phenobarbital

15.00

Richlyn Laboratories Aminophylline & Phenobarbital Tablets 00115-2154 TB Phenobarbital

15.00

Richlyn Laboratories Bellophen 00115-2400 TB Phenobarbital

16.20

Richlyn Laboratories Spasmolin 00115-4652 TB Phenobarbital

15.00

Richwood Pharmaceutical Co., Inc. Bellatal Tablets 58521-0162 TB Phenobarbital, USP

16.20

Roberts Pharmaceutical Corporation Anoquan 54092-0178 TB Butalbital

50.00

Roberts Pharmaceutical Corporation Tencet Tablets 59441-0153 TB Butalbital

50.00

Robins A H Co Inc Donnatal Capsules 00031-4207 CA Phenobarbital

16.20

Robins A H Co Inc Donnatal Extentabs 00031-4235 XT Phenobarbital

48.60

Robins A H Co Inc Donnatal No 2 00031-4264 TB Phenobarbital

32.40

Robins A H Co Inc Donnazyme 00031-4649 ET Phenobarbital

8.10

Roche Labs Menrium 10-4 00140-0025 TB Chlordiazepoxide

10.00

Roche Labs Menrium 5-2 00140-0023 TB Chlordiazepoxide

5.00

Roche Labs Menrium 5-4 00140-0024 TB Chlordiazepoxide

5.00

Rondex Laboratories Antispasmodic 00367-4118 TB Phenobarbital

16.20

Rotex Pharmaceuticals, Inc. Rogesic Capsules 31190-0008 CA Butalbital

50.00

Ruckstuhl Co Sedarex No 3 00144-1575 TB Phenobarbital

16.20

Rugby Laboratories Inc Butalbital, Acetaminophen and Caffeine Tablets, USP 0536-5567 TB Butalbital

50.00

Rugby Laboratories Inc Ergocaff-PB Tablets 00536-3801 TB Pentobarbital Sodium

30.00

Rugby Laboratories Inc Hyosophen Capsules 00536-3926 CA Phenobarbital

16.00

Rugby Laboratories Inc Hyosophen Tablets 00536-3920 TB Phenobarbital

16.20

Rugby Laboratories Inc ISOCET Tablets 00536-3951 TB Butalbital

50.00

Rugby Laboratories Inc Theodrine Tablets 00536-4648 TB Phenobarbital

8.00

Russ Pharmaceuticals, Inc. FEMCET Capsules 50474-0703 CA Butalbital

50.00

Sandoz Pharmaceuticals Belladenal 00078-0028 TB Phenobarbital

50.00

Sandoz Pharmaceuticals Belladenal-S 00078-0027 XT Phenobarbital

50.00

Sandoz Pharmaceuticals Bellergal-S 00078-0031 XT Phenobarbital

40.00

Sandoz Pharmaceuticals Cafergot P-B Suppository 00078-0035 SU Pentobarbital

60.00

Sandoz Pharmaceuticals Cafergot P-B Tablets 00078-0036 TB Pentobarbital Sodium

30.00

Savage Laboratories AXOTAL 00281-1301 TB Butalbital

50.00

Schein Henry Inc Antispasmodic 00364-0020 TB Phenobarbital

16.00

Schein Henry Inc Antispasmodic Elixir 00364-7002 EL Phenobarbital

3.20

Schein Henry Inc Isolate Compound Elixir 00364-7029 EL Phenobarbital

0.40

Schein Henry Inc T-E-P 00364-0266 TB Phenobarbital

8.10

Schein Pharmaceutical, Inc. Chlordiazepoxide HCl and Clidinium Bromide Capsules 00364-0559 CA Chlordiazepoxide Hydrochloride

5.00

9

Exempt Prescription Products

2/21/2020

Company Trade Name NDC Code Form Controlled Substance

(mg or mg/ml)

Shoals Pharmaceuticals, Inc. Tencet 47649-0370 TB Butalbital

50.00

Shoals Pharmaceuticals, Inc. Tencet Capsules 47649-0560 CA Butalbital

50.00

Skylar Laboratories, LLC Allzital (Butalbital and Acetaminophen Tablets) (25 mg/325 mg) 70362-722 TB Butalbital

25.00

Skylar Laboratories, LLC Butalbital and Acetaminophen Tablets (50 mg/325 mg) 70362-721 TB Butalbital

50.00

Solubiomix Butalbital and Acetaminophen Tablets (50 mg/325 mg) 69499-302 TB Butalbital

50.00

Solubiomix Butalbital and Acetaminophen Capsules (50 mg/300 mg) 69499-342 CA Butalbital

50.00

Stewart Jackson Pharmacal, Inc. Ezol 45985-0578 CA Butalbital

50.00

STI Pharma, LLC Butalbital and Acetaminophen Tablets (50 mg/325 mg) 54879-026 TB Butalbital

50.00

Stuart Pharmaceutical Kinesed 00038-0220 TB Phenobarbital

16.00

Sunrise Pharmaceuticals, Inc. Butalbital, Acetaminophen, Caffeine Capsules (50 mg/300 mg/40mg) 11534-187 CA Butalbital

50.00

Superpharm Laboratories Chlordiazepoxide HCl & Clidinium Br 57247-1003 CA Chlordiazepoxide HCl

5.00

Tedor Pharma, Inc. Butalbital and Acetaminophen Tablets (50 mg/300 mg) 47781-534 TB Butalbital

50.00

Tedor Pharma, Inc. Butalbital and Acetaminophen Tablets (50 mg/325 mg) 43199-053 TB Butalbital

50.00

Tedor Pharma, Inc. (Manufactured for Xspire Pharma) Butalbital, Acetaminophen and Caffeine Caps (50mg/300mg/40mg) 42195-955 CA Butalbital

50.00

Teva Pharmaceuticals Chlordiazepoxide HCl & Clidinium Bromide Caps USP (5mg/2.5mg) 0093-3653 CA Chlordiazepoxide HCl

5.00

Towne Paulsen & Co T.E. P. 00157-0980 TB Phenobarbital

8.00

Trimen Labs Amaphen Capsules (reformulated) 11311-0954 CA Butalbital

50.00

Truxton C O Inc Atropine Sulfate with Phenobarbital 00463-6035 TB Phenobarbital

15.00

Truxton C O Inc Ephedrine with Phenobarbital 00463-6086 TB Phenobarbital

15.00

Truxton C O Inc Spastemms Elixir 00463-9023 EL Phenobarbital

3.24

Truxton C O Inc Spastemms Tablets 00463-6181 TB Phenobarbital

15.00

U.S. Pharmaceuticals Medigesic Capsules 52747-0600 CA Butalbital

50.00

UAD Laboratories Inc Bucet Capsules 00785-2307 CA Butalbital

50.00

UDL Laboratories Belladonna Alkaloids with Phenobarbital 51079-0168 TB Phenobarbital

16.20

United Research Laboratories, Inc. Bel-Tabs 00677-1171 TB Phenobarbital

40.00

United Research Laboratories, Inc. Chlordiazepoxide HCl and Clidinium Bromide Capsules 00677-1247 CA Chlordiazepoxide Hydrochloride

5.00

United Research Laboratories, Inc. Hapanol 00677-0074 TB Phenobarbital

16.20

United Research Laboratories, Inc. Theophylline #1 Tablets 00677-0148 TB Phenobarbital

8.00

University of Iowa Bladder Mixture Plus Phenobarbital 11326-1624 LQ Phenobarbital

2.92

US Pharmaceuticals Inc Medigesic Tablets 52747-0311 TB Butalbital

50.00

Vale Chemical Co Alkaloids of Belladonna and Phenobarbital 00377-0527 TB Phenobarbital

16.20

Vale Chemical Co Antispas 00377-0622 TB Phenobarbital

16.20

Vale Chemical Co Barbeloid (Revised) Green 00377-0365 TB Phenobarbital

16.20

Vale Chemical Co Barbeloid Yellow 00377-0498 TB Phenobarbital

16.20

Vale Chemical Co Charspast 00377-0500 TB Phenobarbital

16.20

Vale Chemical Co Digestokraft 00377-0460 TB Butabarbital Sodium

8.00

Vale Chemical Co Ephedrine & Sodium Phenobarbital 00377-0109 TB Phenobarbital Sodium

16.20

Vale Chemical Co Panzyme 00377-0491 TB Phenobarbital

8.10

Vale Chemical Co Pulsaphen 00377-0652 TB Phenobarbital

15.00

Vale Chemical Co Truxaphen 00377-0541 TB Phenobarbital

16.20

10

Exempt Prescription Products

2/21/2020

Company Trade Name NDC Code Form Controlled Substance

(mg or mg/ml)

Vale Chemical Co Wescophen S-II 00377-0628 TB Phenobarbital

30.00

Vale Chemical Co Wesmatic Forte 00377-0426 TB Phenobarbital

8.10

Valeant Pharmaceuticals Phrenilin Forte 0187-0844 CA Butalbital

50.00

Valeant Pharmaceuticals International Librax (Chlordiazepoxide HCl and Clidinium Bromide) Capsules 0187-4100 CA Chlordiazepoxide HCl

5.00

Valeant Pharmaceuticals Intl./Oceanside Pharmaceuticals Inc. Chlordiazepoxide HCl and Clidinium Bromide Capsules 68682-409 CA Chlordiazepoxide HCl

5.00

Victory Pharma Inc. (Manuf. By West-Ward Pharmaceutical) Zebutal Brand Butalbital, Acetaminophen, and Caffeine Capsules 68453-170 CA Butalbital

50.00

Vintage Pharmaceuticals Chlordiazepoxide Hydrochloride and Clidinium Bromide Capsules 0254-2732 CA Chlordiazepoxide

5.00

Vistapharm, Inc. Donnatal Elixir Grape Flavor 5ml Unit Dose 66689-0063 LQ Phenobarbital

16.20

Vitarine Pharmaceuticals, Inc E-Caff PB Tablets 00185-0982 TB Pentobarbital

30.00

Vortech Pharmacal Co Donna-Sed 00298-5054 EL Phenobarbital

3.24

Vortech Pharmacal Co Hypnaldyne 00298-1778 TB Phenobarbital

16.20

Vortech Pharmacal Co Isophed 00298-5680 LQ Phenobarbital

0.40

Vortech Pharmacal Co Phedral C. T. 00298-1173 TB Phenobarbital

8.10

Wallace Laboratories Barbidonna Elixir 00037-0305 EL Phenobarbital

3.20

Wallace Laboratories Barbidonna No 2 00037-0311 TB Phenobarbital

32.00

Wallace Laboratories Barbidonna Tablets 00037-0301 TB Phenobarbital

16.00

Wallace Laboratories Butibel Elixir 00037-0044 EL Butabarbital Sodium

3.00

Wallace Laboratories Butibel Tablets 00037-0046 TB Butabarbital Sodium

15.00

Wallace Laboratories Lufyllin-EPG Elixir 00037-0565 EL Phenobarbital

1.60

Wallace Laboratories Lufyllin-EPG Tablets 00037-0561 TB Phenobarbital

16.00

Wallace Laboratories Milprem-200 00037-5501 TB Meprobamate

200.00

Wallace Laboratories Milprem-400 00037-5401 TB Meprobamate

400.00

Warner Chilcott Laboratories Pyridium Plus Tablets 00430-0182 TB Butabarbital

15.00

WE Hauck Inc G-1 Capsules 43797-0244 CA Butalbital

50.00

Wesley Pharmacal Co Hytrophen 00917-0244 TB Phenobarbital

16.20

Wesley Pharmacal Co Pulsaphen Gray 00917-0113 TB Phenobarbital

15.00

Wesley Pharmacal Co Wescophen-S 00917-0135 TB Phenobarbital

30.00

Wesley Pharmacal Co Wesmatic Forte 00917-0845 TB Phenobarbital

8.00

Westminster Pharmaceuticals Butalbital, Acetaminophen and Caffeine Tablets(50mg/325mg/40mg) 69367-203 TB Butalbital

50.00

West-Ward Pharmaceutical Corp. Belladonna Alkaloids & Phenobarbital 00143-1140 TB Phenobarbital

16.20

West-Ward Pharmaceutical Corp. Butalbital with Acetaminophen and Caffeine Tablets 00143-1787 TB Butalbital

50.00

West-Ward Pharmaceutical Corp. Butalbital, Acetaminophen and Caffein Capsules 00143-3001 CA Butalbital

50.00

West-Ward Pharmaceutical Corp. Butalbital, Acetaminophen, and Caffeine Tablets, USP 00143-1115 TB Butalbital

50.00

West-Ward Pharmaceutical Corp. Clindinax Capsules 00143-3091 CA Chlordiazepoxide Hydrochloride

5.00

West-Ward Pharmaceutical Corp. Clindinax Capsules 00143-3092 CA Chlordiazepoxide Hydrochloride

5.00

West-Ward Pharmaceutical Corp. Theophylline Ephedrine & Phenobarbital 00143-1695 TB Phenobarbital

8.00

West-Ward Pharmaceutical Corp. Zebutal Brand Butalbital, Acetaminophen, and Caffeine Capsules 59630-0170 CA Butalbital

50.00

Winder Laboratories, LLC. Phenohytro (Phenobarbital, Hyoscyamine, Atropine, Scopolamine) 75826-118 TB Phenobarbital

16.20

Winder Laboratories, LLC. Phenohytro (Phenobarbital, Hyoscyamine, Atropine, Scopolamine) 75826-127 LQ Phenobarbital

16.20

Winder Laboratories, LLC. Phenohytro (Phenobarbital, Hyoscyamine, Atropine, Scopolamine) 75826-128 LQ Phenobarbital

16.20

11.

Exempt Prescription Products

2/21/2020

Company Trade Name NDC Code Form Controlled Substance

(mg or mg/ml)

Winthrop Labs Isuprel 00024-0874 EL Phenobarbital

0.40

Wraser Pharmaceuticals Phrenilin Forte (Butalbital, Acetaminophen and Caffeine) 50/300/40 66992-955 CA Butalbital

50.00

Zenith Goldline Pharmaceuticals Belladonna Alkaloids with Phenobarbital ER Tablets 00182-2611 TB Phenobarbital

48.60

Zenith Goldline Pharmaceuticals Butalbital, Acetaminophen and Caffeine Tablets 00182-2659 TB Butalbital

50.00

Zenith Labs Inc Azpan 00172-3747 TB Phenobarbital

8.00

Zenith Labs Inc Chlordiazepoxide HCl and Clidinium Bromide Capsules, USP 00172-2982 CA Chlordiazepoxide HCl

5.00

Come From:
https://www.deadiversion.usdoj.gov/schedules/exempt/exempt_rx_list.pdf