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Bupropion Hydrochloride - 49349-726-02 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 49349-726
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
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 49349-726
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077715
Marketing Category: ANDA
Start Marketing Date: 20110825

Package Information of Bupropion Hydrochloride

Package NDC: 49349-726-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-726-02)

NDC Information of Bupropion Hydrochloride

NDC Code 49349-726-02
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-726-02)
Product NDC 49349-726
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110825
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 Hydrochloride


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