BENZPHETAMINE HYDROCHLORIDE description, usages, side effects, indications, overdosage, supplying and lots more!

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BENZPHETAMINE HYDROCHLORIDE

PD-Rx Pharmaceuticals, Inc.
PD-Rx Pharmaceuticals, Inc.

BENZPHETAMINE HYDROCHLORIDE 50MG USP CIII RX ONLY


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BENZPHETAMINE HYDROCHLORIDE DESCRIPTION



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BENZPHETAMINE HYDROCHLORIDE



CLINICAL PHARMACOLOGY

Benzphetamine hydrochloride is a sympathomimetic amine with pharmacologic activity similar to the prototype drugs of this class used in obesity, the amphetamines. Actions include central nervous system stimulation and elevation of blood pressure. Tachyphylaxis and tolerance have been demonstrated with all drugs of this class in which these phenomena have been looked for.

Drugs of this class used in obesity are commonly known as "anorectics" or "anorexigenics". It has not been established, however, that the action of such drugs in treating obesity is primarily one of appetite suppression. Other central nervous system actions, or metabolic effects, may be involved.

Adult obese subjects instructed in dietary management and treated with "anorectic" drugs, lose more weight on the average than those treated with placebo and diet, as determined in relatively short-term clinical trials.

The magnitude of increased weight loss of drug-treated patients over placebo-treated patients is only a fraction of a pound a week. The rate of weight loss is the greatest in the first weeks of therapy for both drug and placebo subjects and tends to decrease in succeeding weeks. The possible origins of the increased weight loss due to the various drug effects are not established. The amount of weight loss associated with the use of an "anorectic" drug varies from trial to trial, and the increased weight loss appears to be related in part to variables other than the drug prescribed, such as the physician-investigator, the population treated, and the diet prescribed. Studies do not permit conclusions as to the relative importance of the drug and non-drug factors on weight loss.

The natural history of obesity is measured in years, whereas the studies cited are restricted to a few weeks duration; thus, the total impact of drug-induced weight loss over that of diet alone must be considered to be clinically limited.



PHARMACOKINETICS


INDICATION AND USAGE

(see CLINICAL PHARMACOLOGY)

BENZPHETAMINE HYDROCHLORIDE CONTRAINDICATIONS

Benzphetamine Hydrochloride Tablets are contraindicated in patients with advanced arteriosclerosis, symptomatic cardiovascular disease, moderate to severe hypertension, hyperthyroidism, known hypersensitivity or idiosyncrasy to sympathomimetic amines, and glaucoma. Benzphetamine should not be given to patients who are in an agitated state or who have a history of drug abuse.

Hypertensive crises have resulted when sympathomimetic amines have been used concomitantly or within 14 days following use of monoamine oxidase inhibitors. Benzphetamine Hydrochloride Tablets should not be used concomitantly with other CNS stimulants.

Benzphetamine Hydrochloride Tablets may cause fetal harm when administered to a pregnant woman. Amphetamines have been shown to be teratogenic and embryotoxic in mammals at high multiples of the human dose. Benzphetamine Hydrochloride Tablets are contraindicated in women who are or may become pregnant. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus.

WARNINGS

PRECAUTIONS

General







Information For Patients



Drug Interactions






Carcinogenesis, Mutagenesis, Impairment of Fertility


Pregnancy

(see CONTRAINDICATIONS section).

Nursing Mothers


Pediatric Use


BENZPHETAMINE HYDROCHLORIDE ADVERSE REACTIONS


Cardiovascular:

CNS:


Gastrointestinal:

Allergic:

Endocrine:



DRUG ABUSE AND DEPENDENCE














OVERDOSAGE

Manifestations of Overdosage:






Treatment of Overdosage:(see WARNINGS)










DOSAGE & ADMINISTRATION







STORAGE AND HANDLING



PACKAGE LABEL,PRINCIPAL DISPLAY PANEL

56 Tablets NDC 12634-118-56
Benzphetamine Tablets USP
CIII
50mg
Rx Only

Each Tablet Contains:

Usual Adult Dosage:


Keep This and all Medication Out of Reach of Children.






Repackaged and Distributed by
Apotheca, Inc.
Phoenix, AZ 85006

BENZPHETAMINE HYDROCHLORIDE






BENZPHETAMINE HYDROCHLORIDE

BENAPHETAMINE TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:55289-158(NDC:64376-650)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZPHETAMINE HYDROCHLORIDE BENZPHETAMINE 50 mg

Inactive Ingredients

Ingredient Name Strength
CALCIUM STEARATE
polyethylene glycol
FD&C YELLOW NO. 6
ANHYDROUS LACTOSE
sorbitol

Product Characteristics

Color Size Imprint Code Shape
orange (PEACH) 8 mm BP;650 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55289-158-14 14 in 1 BOTTLE, PLASTIC
2 NDC:55289-158-60 60 in 1 BOTTLE, PLASTIC
3 NDC:55289-158-28 28 in 1 BOTTLE, PLASTIC
4 NDC:55289-158-56 56 in 1 BOTTLE, PLASTIC
5 NDC:55289-158-90 90 in 1 BOTTLE, PLASTIC
6 NDC:55289-158-30 30 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040747 2009-12-09


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