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Bupropion Hydrochloride - 64679-102-01 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 64679-102
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: 64679-102
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202189
Marketing Category: ANDA
Start Marketing Date: 20121121

Package Information of Bupropion Hydrochloride

Package NDC: 64679-102-01
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-01)

NDC Information of Bupropion Hydrochloride

NDC Code 64679-102-01
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-01)
Product NDC 64679-102
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 20121121
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
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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