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Benzphetamine Hydrochloride - 63629-4139-4 - (Benzphetamine Hydrochloride)

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Drug Information of Benzphetamine Hydrochloride

Product NDC: 63629-4139
Proprietary Name: Benzphetamine Hydrochloride
Non Proprietary Name: Benzphetamine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Benzphetamine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Benzphetamine Hydrochloride

Product NDC: 63629-4139
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040845
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of Benzphetamine Hydrochloride

Package NDC: 63629-4139-4
Package Description: 21 TABLET in 1 BOTTLE (63629-4139-4)

NDC Information of Benzphetamine Hydrochloride

NDC Code 63629-4139-4
Proprietary Name Benzphetamine Hydrochloride
Package Description 21 TABLET in 1 BOTTLE (63629-4139-4)
Product NDC 63629-4139
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzphetamine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
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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