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Bupropion HydrochlorideXL - 52125-508-02 - (Bupropion Hydrochloride)

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Drug Information of Bupropion HydrochlorideXL

Product NDC: 52125-508
Proprietary Name: Bupropion HydrochlorideXL
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 300    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 HydrochlorideXL

Product NDC: 52125-508
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077715
Marketing Category: ANDA
Start Marketing Date: 20130603

Package Information of Bupropion HydrochlorideXL

Package NDC: 52125-508-02
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52125-508-02)

NDC Information of Bupropion HydrochlorideXL

NDC Code 52125-508-02
Proprietary Name Bupropion HydrochlorideXL
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52125-508-02)
Product NDC 52125-508
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 20130603
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 300
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 HydrochlorideXL


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