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Bupropion hydrochloride - 47335-737-13 - (Bupropion hydrochloride)

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Drug Information of Bupropion hydrochloride

Product NDC: 47335-737
Proprietary Name: Bupropion hydrochloride
Non Proprietary Name: Bupropion hydrochloride
Active Ingredient(s): 150    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: 47335-737
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078866
Marketing Category: ANDA
Start Marketing Date: 20100408

Package Information of Bupropion hydrochloride

Package NDC: 47335-737-13
Package Description: 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-13)

NDC Information of Bupropion hydrochloride

NDC Code 47335-737-13
Proprietary Name Bupropion hydrochloride
Package Description 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-13)
Product NDC 47335-737
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 20100408
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 150
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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