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Bupropion Hydrochloride - 55648-107-03 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 55648-107
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: 55648-107
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201331
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of Bupropion Hydrochloride

Package NDC: 55648-107-03
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-107-03)

NDC Information of Bupropion Hydrochloride

NDC Code 55648-107-03
Proprietary Name Bupropion Hydrochloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-107-03)
Product NDC 55648-107
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 20120830
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
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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