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Diethylpropion HCl Immediate-Release - 54569-2059-7 - (Diethylpropion hydrochloride)

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Drug Information of Diethylpropion HCl Immediate-Release

Product NDC: 54569-2059
Proprietary Name: Diethylpropion HCl Immediate-Release
Non Proprietary Name: Diethylpropion hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Diethylpropion hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diethylpropion HCl Immediate-Release

Product NDC: 54569-2059
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011722
Marketing Category: NDA
Start Marketing Date: 19590806

Package Information of Diethylpropion HCl Immediate-Release

Package NDC: 54569-2059-7
Package Description: 60 TABLET in 1 BOTTLE (54569-2059-7)

NDC Information of Diethylpropion HCl Immediate-Release

NDC Code 54569-2059-7
Proprietary Name Diethylpropion HCl Immediate-Release
Package Description 60 TABLET in 1 BOTTLE (54569-2059-7)
Product NDC 54569-2059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diethylpropion hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19590806
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
Substance Name DIETHYLPROPION HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Diethylpropion HCl Immediate-Release


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