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DIETHYLPROPION HYDROCHLORIDE - 50436-4164-1 - (DIETHYLPROPION HYDROCHLORIDE)

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Drug Information of DIETHYLPROPION HYDROCHLORIDE

Product NDC: 50436-4164
Proprietary Name: DIETHYLPROPION HYDROCHLORIDE
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 HYDROCHLORIDE

Product NDC: 50436-4164
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201212
Marketing Category: ANDA
Start Marketing Date: 20101227

Package Information of DIETHYLPROPION HYDROCHLORIDE

Package NDC: 50436-4164-1
Package Description: 21 TABLET in 1 BOTTLE (50436-4164-1)

NDC Information of DIETHYLPROPION HYDROCHLORIDE

NDC Code 50436-4164-1
Proprietary Name DIETHYLPROPION HYDROCHLORIDE
Package Description 21 TABLET in 1 BOTTLE (50436-4164-1)
Product NDC 50436-4164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIETHYLPROPION HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101227
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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 HYDROCHLORIDE


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