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Bupropion Hydrochloride - 54868-5377-1 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 54868-5377
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 54868-5377
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075932
Marketing Category: ANDA
Start Marketing Date: 20070410

Package Information of Bupropion Hydrochloride

Package NDC: 54868-5377-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5377-1)

NDC Information of Bupropion Hydrochloride

NDC Code 54868-5377-1
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5377-1)
Product NDC 54868-5377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070410
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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