Bupropion - 54868-5927-1 - (bupropion hydrochloride)

Alphabetical Index


Drug Information of Bupropion

Product NDC: 54868-5927
Proprietary Name: Bupropion
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

Product NDC: 54868-5927
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077715
Marketing Category: ANDA
Start Marketing Date: 20080813

Package Information of Bupropion

Package NDC: 54868-5927-1
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5927-1)

NDC Information of Bupropion

NDC Code 54868-5927-1
Proprietary Name Bupropion
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5927-1)
Product NDC 54868-5927
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bupropion hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080813
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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


General Information