PRINCIPAL DISPLAY PANEL - 97.2 mg Tablet Bottle Label

PHENOBARBITAL
TABLETS-CA1
CIV

Antiepileptic for
oral use in dogs only.

97.2 mg

Conditionally approved by FDA
pending a full demonstration of effectiveness
under application number 141-578.
It is a violation of federal law to use this
product other than as directed on the labeling.

Net Contents: 100 tablets
NDC 51672-5325-1

TARO

INDICATION:

PHENOBARBITAL TABLETS-CA1 are indicated for the control of seizures associated with idiopathic epilepsy in dogs.

CONTRAINDICATIONS:

PHENOBARBITAL TABLETS-CA1 should not be used in animals with a history of hypersensitivity to phenobarbital.

ADVERSE REACTIONS:

Based on a comprehensive review of publications evaluating phenobarbital, the following adverse reactions are associated with administration of phenobarbital:

General: ataxia, lethargy, increased water consumption, increased appetite, increased urination, hyperactivity, vomiting, diarrhea, and weight gain.

Hematologic: increased serum alkaline phosphatase (ALP), increased serum alanine transferase (ALT), increased serum gamma-glutamyl transferase (GGT), decreased serum total and free thyroxine (T4) concentrations, immune-mediated anemia, neutropenia, and thrombocytopenia. Rarely, idiosyncratic hepatotoxicity may also occur.

A retrospective study of data on 1083 cases from a poison control center included 268 dogs that ingested phenobarbital alone at a dose of ≤5 mg/kg. Among the 22 dogs with at least one adverse reaction, the following were the most common adverse reactions observed: drowsiness/lethargy, ataxia, agitated/irritable, vocalization, unable to rise, and vomiting. Each of these adverse reactions were reported in 2 or more dogs.

Manufactured for:Taro Pharmaceuticals U.S.A. Inc.
Hawthorne, NY 10532

Revised: March 2024

DESCRIPTION:

PHENOBARBITAL TABLETS-CA1 is an unflavored, bisected tablet that contains phenobarbital. Phenobarbital is white, odorless, small crystals or white crystalline powder with a bitter taste. The molar mass of phenobarbital is 232.235 g/mol, with solubility in water, alcohol, ether, and in fixed alkali hydroxides and carbonates.

DOSAGE AND ADMINISTRATION:

PHENOBARBITAL TABLETS-CA1 is given orally twice a day at the minimum dosage of 2.5 mg/kg and may be titrated to effect to a maximum dosage of 5 mg/kg. The dosage of PHENOBARBITAL TABLETS-CA1 should be adjusted based on monitoring the clinical response of the individual patient. PHENOBARBITAL TABLETS-CA1 should be dosed with food.

All split tablets should be used within 90 days.

WARNINGS:

Human Safety Warnings

Not for use in humans. Keep this and all medications out of reach of children.

Because phenobarbital may cause developmental effects, women who are pregnant or may become pregnant should handle and administer PHENOBARBITAL TABLETS-CA1 with caution.

Human User Safety While Handling PHENOBARBITAL TABLETS-CA1

Mucous Membrane Contact, Eye Contact, or Accidental Ingestion:

In case of accidental ingestion, skin reaction, or eye exposure, contact a physician immediately.

If accidental eye contact or mucous membrane exposure occurs, rinse the exposed area thoroughly.

Skin Contact:

Users should wash skin exposed to the drug, including washing their hands thoroughly after contacting the drug.

Drug Abuse, Addiction, and Diversion

Controlled Substance:

PHENOBARBITAL TABLETS-CA1 contains phenobarbital, a Schedule IV controlled substance.

Abuse: Phenobarbital is a barbiturate and a central nervous system (CNS) depressant with a potential for misuse, abuse, and addiction. Abuse is defined as the intentional, non-therapeutic use of a drug, even once, to achieve a desired psychological or physiological effect. Misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider. Drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug use (e.g., continuing drug use despite harmful consequences, giving a higher priority to drug use than other activities and obligations), and possible tolerance or physical dependence.

Abuse and misuse of barbiturates often (but not always) involve the use of doses exceeding the doses used in clinical practice and commonly involve concomitant use of other medications, alcohol, and/or illicit substances, which is associated with an increased frequency of serious adverse outcomes, including respiratory depression, overdose, or death. Barbiturates, including phenobarbital, are often sought by individuals who abuse drugs and other substances, and by individuals with addictive disorders.

Symptoms of acute intoxication with barbiturates include unsteady gait, slurred speech, and sustained nystagmus. Mental signs of chronic intoxication include confusion, poor judgment, irritability, insomnia, and somatic complaints. The use of phenobarbital alone can result in death; however, death is more often associated with phenobarbital use in the context of polysubstance use (especially with other CNS depressants, such as opioids and alcohol).

Phenobarbital may produce physical dependence. Physical dependence is a state that develops as a result of physiological adaptation in response to repeated drug use, manifested by withdrawal signs and symptoms after abrupt discontinuation or a significant dose reduction of a drug. Abrupt discontinuation or rapid dosage reduction of phenobarbital may precipitate acute withdrawal reactions, including seizures, which can be life-threatening.

Tolerance may occur with continued use. As tolerance to barbiturates develops, the amount needed to maintain the same level of intoxication increases; tolerance to a fatal dosage, however, does not increase more than twofold. As this occurs, the margin between intoxicating dosage and fatal dosage becomes smaller.

Consider the potential risks of misuse or abuse before prescribing this product. Signs of phenobarbital misuse or abuse include drug seeking behavior.

Diversion: PHENOBARBITAL TABLETS-CA1 is a Schedule IV antiepileptic and should be handled appropriately to minimize the risk of diversion, including restriction of access, the use of accounting procedures, and proper disposal methods. Store in a locked cabinet according to federal and state controlled substance requirements and guidelines. Any unused or expired bottles must be destroyed by a reverse distributor. For further information, contact your local DEA field office or call Genus Lifesciences Inc. at 1-833-599-7582.

Note to physician: PHENOBARBITAL TABLETS-CA1 contains phenobarbital.

Users can call Genus Lifesciences Inc. at 1-833-599-7582 at any time for product safety support. To obtain a Safety Data Sheet(s), contact Genus Lifesciences Inc. at 1-833-599-7582 or at https://www.genuslifesciences.com.

Animal Safety Warnings

Not for use in cats.

Do not use in pregnant or lactating dogs. Based on data from laboratory animals, administration of PHENOBARBITAL TABLETS-CA1 to pregnant dogs may produce congenital malformations in the developing fetus. Phenobarbital may be present and accumulate in the milk of lactating dogs.

Keep PHENOBARBITAL TABLETS-CA1 in a secure location out of the reach of dogs, cats, or other animals to prevent accidental ingestion or overdose.

PRECAUTIONS:

PHENOBARBITAL TABLETS-CA1 is for use in dogs 6 months of age and older.

The safe use of PHENOBARBITAL TABLETS-CA1 in neonates and young dogs has not been established.

Careful monitoring of therapeutic, biochemical, and hematology parameters is important in dogs receiving PHENOBARBITAL TABLETS-CA1. Dogs receiving PHENOBARBITAL TABLETS-CA1 should also be carefully monitored when administering concurrent medications.

Dogs with decreased liver function may be predisposed to phenobarbital toxicosis.

Some dogs may experience epileptic episodes that are refractory or unresponsive to PHENOBARBITAL TABLETS-CA1 monotherapy.

Dogs should be monitored for adverse events when adjusting the dose to determine the optimal dose for each patient.

The safe use of PHENOBARBITAL TABLETS-CA1 has not been evaluated in dogs that are intended for breeding, or that are pregnant or lactating.

CLINICAL PHARMACOLOGY:

Mechanism of Action: Phenobarbital is a barbiturate thought to exert its antiepileptic activity by enhancing the action of gamma-aminobutyric acid (GABA) through binding to a site on the GABAA receptor/chloride channel. Barbiturates are also thought to decrease the influx of calcium into nerve cells and thereby decrease release of neurotransmitters.

Pharmacokinetics: The pharmacokinetics of phenobarbital in dogs have been described in published literature. Phenobarbital is considered a lipid-soluble drug exhibiting fast first-order absorption, high systemic availability, wide distribution, extensive hepatic metabolism, and slow and variable elimination from the body. Mean terminal elimination half-lives have been reported to range between 30 and 90 hours after oral administration. Half-lives tend to decrease after weeks of continuous administration. Steady state concentrations are often achieved after 2 or more weeks of daily or twice daily dosing. Phenobarbital has been reported to undergo self-induction of microsomal metabolism after weeks or months of daily administration, often requiring adjusting the dose after a certain period of time.

HOW SUPPLIED:

PHENOBARBITAL TABLETS-CA1 are unflavored, bisected tablets containing 16.2, 32.4, 64.8, and 97.2 mg phenobarbital per tablet. PHENOBARBITAL TABLETS-CA1 are packaged in bottles of 100, 500 or 1000 tablets.

STORAGE CONDITIONS:

Store at 25°C (77°F) with excursions permitted between 15° to 30°C (59° to 86°F).