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Diethylpropion Hydrochloride - 0527-1477-25 - (Diethylpropion Hydrochloride)

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Drug Information of Diethylpropion Hydrochloride

Product NDC: 0527-1477
Proprietary Name: Diethylpropion Hydrochloride
Non Proprietary Name: Diethylpropion Hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Diethylpropion Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diethylpropion Hydrochloride

Product NDC: 0527-1477
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091680
Marketing Category: ANDA
Start Marketing Date: 20111024

Package Information of Diethylpropion Hydrochloride

Package NDC: 0527-1477-25
Package Description: 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-25)

NDC Information of Diethylpropion Hydrochloride

NDC Code 0527-1477-25
Proprietary Name Diethylpropion Hydrochloride
Package Description 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-25)
Product NDC 0527-1477
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diethylpropion Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111024
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
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 Hydrochloride


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