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Bupropion Hydrochloride - 63629-3332-1 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 63629-3332
Proprietary Name: Bupropion Hydrochloride
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Bupropion Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 63629-3332
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076711
Marketing Category: ANDA
Start Marketing Date: 20041203

Package Information of Bupropion Hydrochloride

Package NDC: 63629-3332-1
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3332-1)

NDC Information of Bupropion Hydrochloride

NDC Code 63629-3332-1
Proprietary Name Bupropion Hydrochloride
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3332-1)
Product NDC 63629-3332
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041203
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of Bupropion Hydrochloride


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