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Benzphetamine Hydrochloride - 0574-0116-30 - (BENZPHETAMINE HYDROCHLORIDE)

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Drug Information of Benzphetamine Hydrochloride

Product NDC: 0574-0116
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benzphetamine Hydrochloride

Product NDC: 0574-0116
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040578
Marketing Category: ANDA
Start Marketing Date: 20070501

Package Information of Benzphetamine Hydrochloride

Package NDC: 0574-0116-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (0574-0116-30)

NDC Information of Benzphetamine Hydrochloride

NDC Code 0574-0116-30
Proprietary Name Benzphetamine Hydrochloride
Package Description 30 TABLET, COATED in 1 BOTTLE (0574-0116-30)
Product NDC 0574-0116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZPHETAMINE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20070501
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, 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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