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Bupropion hydrochloride - 67767-117-60 - (Bupropion hydrochloride)

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Drug Information of Bupropion hydrochloride

Product NDC: 67767-117
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion hydrochloride

Product NDC: 67767-117
Labeler Name: Actavis South Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077475
Marketing Category: ANDA
Start Marketing Date: 20080312

Package Information of Bupropion hydrochloride

Package NDC: 67767-117-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-117-60)

NDC Information of Bupropion hydrochloride

NDC Code 67767-117-60
Proprietary Name Bupropion hydrochloride
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-117-60)
Product NDC 67767-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080312
Marketing Category Name ANDA
Labeler Name Actavis South Atlantic 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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