Home > National Drug Code (NDC) > Bupropion Hydrochloride

Bupropion Hydrochloride - 21695-578-30 - (Bupropion Hydrochloride)

Alphabetical Index


Drug Information of Bupropion Hydrochloride

Product NDC: 21695-578
Proprietary Name: Bupropion Hydrochloride
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 300    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: 21695-578
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077715
Marketing Category: ANDA
Start Marketing Date: 20070613

Package Information of Bupropion Hydrochloride

Package NDC: 21695-578-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-578-30)

NDC Information of Bupropion Hydrochloride

NDC Code 21695-578-30
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-578-30)
Product NDC 21695-578
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 20070613
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 300
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


General Information