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Bupropion Hydrochloride - 49349-774-02 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 49349-774
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
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 49349-774
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075491
Marketing Category: ANDA
Start Marketing Date: 20110908

Package Information of Bupropion Hydrochloride

Package NDC: 49349-774-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-774-02)

NDC Information of Bupropion Hydrochloride

NDC Code 49349-774-02
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-774-02)
Product NDC 49349-774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110908
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


General Information