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Diethylpropion HCl Immediate-Release - 68387-695-21 - (Diethylpropion hydrochloride)

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Drug Information of Diethylpropion HCl Immediate-Release

Product NDC: 68387-695
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: 68387-695
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA011722
Marketing Category: ANDA
Start Marketing Date: 20100607

Package Information of Diethylpropion HCl Immediate-Release

Package NDC: 68387-695-21
Package Description: 21 TABLET in 1 BOTTLE, PLASTIC (68387-695-21)

NDC Information of Diethylpropion HCl Immediate-Release

NDC Code 68387-695-21
Proprietary Name Diethylpropion HCl Immediate-Release
Package Description 21 TABLET in 1 BOTTLE, PLASTIC (68387-695-21)
Product NDC 68387-695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diethylpropion hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100607
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals 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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