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Bupropion Hydrochloride - 21695-018-30 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 21695-018
Proprietary Name: Bupropion Hydrochloride
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Bupropion Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 21695-018
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075584
Marketing Category: ANDA
Start Marketing Date: 20000207

Package Information of Bupropion Hydrochloride

Package NDC: 21695-018-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-018-30)

NDC Information of Bupropion Hydrochloride

NDC Code 21695-018-30
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-018-30)
Product NDC 21695-018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000207
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 100
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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