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Bupropion Hydrochloride - 49349-270-02 - (BUPROPION HYDROCHLORIDE)

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Drug Information of Bupropion Hydrochloride

Product NDC: 49349-270
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 49349-270
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077715
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of Bupropion Hydrochloride

Package NDC: 49349-270-02
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49349-270-02)

NDC Information of Bupropion Hydrochloride

NDC Code 49349-270-02
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49349-270-02)
Product NDC 49349-270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUPROPION HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120830
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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