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Diethylpropion HCl Controlled-Release - 21695-876-30 - (Diethylpropion hydrochloride)

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Drug Information of Diethylpropion HCl Controlled-Release

Product NDC: 21695-876
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: 21695-876
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011722
Marketing Category: NDA
Start Marketing Date: 20080101

Package Information of Diethylpropion HCl Controlled-Release

Package NDC: 21695-876-30
Package Description: 30 TABLET in 1 BOTTLE (21695-876-30)

NDC Information of Diethylpropion HCl Controlled-Release

NDC Code 21695-876-30
Proprietary Name Diethylpropion HCl Controlled-Release
Package Description 30 TABLET in 1 BOTTLE (21695-876-30)
Product NDC 21695-876
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diethylpropion hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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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