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BENZPHETAMINE hYDROCHLORIDE - 12634-118-44 - (BENAPHETAMINE)

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Drug Information of BENZPHETAMINE hYDROCHLORIDE

Product NDC: 12634-118
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: 12634-118
Labeler Name: Apotheca Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040747
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of BENZPHETAMINE hYDROCHLORIDE

Package NDC: 12634-118-44
Package Description: 84 TABLET in 1 BOTTLE, PLASTIC (12634-118-44)

NDC Information of BENZPHETAMINE hYDROCHLORIDE

NDC Code 12634-118-44
Proprietary Name BENZPHETAMINE hYDROCHLORIDE
Package Description 84 TABLET in 1 BOTTLE, PLASTIC (12634-118-44)
Product NDC 12634-118
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 Apotheca 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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