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Diethylpropion HCl Controlled-Release - 54569-0396-5 - (Diethylpropion hydrochloride)

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Drug Information of Diethylpropion HCl Controlled-Release

Product NDC: 54569-0396
Proprietary Name: Diethylpropion HCl Controlled-Release
Non Proprietary Name: Diethylpropion hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Diethylpropion hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diethylpropion HCl Controlled-Release

Product NDC: 54569-0396
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012546
Marketing Category: NDA
Start Marketing Date: 19601117

Package Information of Diethylpropion HCl Controlled-Release

Package NDC: 54569-0396-5
Package Description: 28 TABLET in 1 BOTTLE (54569-0396-5)

NDC Information of Diethylpropion HCl Controlled-Release

NDC Code 54569-0396-5
Proprietary Name Diethylpropion HCl Controlled-Release
Package Description 28 TABLET in 1 BOTTLE (54569-0396-5)
Product NDC 54569-0396
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diethylpropion hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19601117
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
Substance Name DIETHYLPROPION HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Diethylpropion HCl Controlled-Release


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