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Diethylpropion HCl Immediate-Release - 0591-0783-01 - (Diethylpropion hydrochloride)

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Drug Information of Diethylpropion HCl Immediate-Release

Product NDC: 0591-0783
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: 0591-0783
Labeler Name: Watson Laboratories, Inc.
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: 0591-0783-01
Package Description: 100 TABLET in 1 BOTTLE (0591-0783-01)

NDC Information of Diethylpropion HCl Immediate-Release

NDC Code 0591-0783-01
Proprietary Name Diethylpropion HCl Immediate-Release
Package Description 100 TABLET in 1 BOTTLE (0591-0783-01)
Product NDC 0591-0783
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 Watson Laboratories, Inc.
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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