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BENZPHETAMINE HYDROCHLORIDE - 55289-158-28 - (BENAPHETAMINE)

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Drug Information of BENZPHETAMINE HYDROCHLORIDE

Product NDC: 55289-158
Proprietary Name: BENZPHETAMINE HYDROCHLORIDE
Non Proprietary Name: BENAPHETAMINE
Active Ingredient(s): 50    mg/1 & nbsp;   BENAPHETAMINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of BENZPHETAMINE HYDROCHLORIDE

Product NDC: 55289-158
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040747
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of BENZPHETAMINE HYDROCHLORIDE

Package NDC: 55289-158-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (55289-158-28)

NDC Information of BENZPHETAMINE HYDROCHLORIDE

NDC Code 55289-158-28
Proprietary Name BENZPHETAMINE HYDROCHLORIDE
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (55289-158-28)
Product NDC 55289-158
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENAPHETAMINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091209
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name BENZPHETAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of BENZPHETAMINE HYDROCHLORIDE


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