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Bupropion Hydrochloride - 67767-135-60 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 67767-135
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: 67767-135
Labeler Name: Actavis South Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077455
Marketing Category: ANDA
Start Marketing Date: 20100719

Package Information of Bupropion Hydrochloride

Package NDC: 67767-135-60
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67767-135-60)

NDC Information of Bupropion Hydrochloride

NDC Code 67767-135-60
Proprietary Name Bupropion Hydrochloride
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67767-135-60)
Product NDC 67767-135
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 20100719
Marketing Category Name ANDA
Labeler Name Actavis South Atlantic LLC
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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