DIDREX - 54569-0389-6 - (benzphetamine hydrochloride)

Alphabetical Index


Drug Information of DIDREX

Product NDC: 54569-0389
Proprietary Name: DIDREX
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 DIDREX

Product NDC: 54569-0389
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012427
Marketing Category: NDA
Start Marketing Date: 19601026

Package Information of DIDREX

Package NDC: 54569-0389-6
Package Description: 90 TABLET in 1 BOTTLE (54569-0389-6)

NDC Information of DIDREX

NDC Code 54569-0389-6
Proprietary Name DIDREX
Package Description 90 TABLET in 1 BOTTLE (54569-0389-6)
Product NDC 54569-0389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzphetamine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19601026
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
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 DIDREX


General Information