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benzphetamine hydrochloride - 43063-425-30 - (benzphetamine hydrochloride)

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Drug Information of benzphetamine hydrochloride

Product NDC: 43063-425
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: 43063-425
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090473
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of benzphetamine hydrochloride

Package NDC: 43063-425-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-425-30)

NDC Information of benzphetamine hydrochloride

NDC Code 43063-425-30
Proprietary Name benzphetamine hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-425-30)
Product NDC 43063-425
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzphetamine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
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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