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buPROPion Hydrochloride - 63739-450-10 - (buPROPion Hydrochloride)

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Drug Information of buPROPion Hydrochloride

Product NDC: 63739-450
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: 63739-450
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077285
Marketing Category: ANDA
Start Marketing Date: 20110221

Package Information of buPROPion Hydrochloride

Package NDC: 63739-450-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-450-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of buPROPion Hydrochloride

NDC Code 63739-450-10
Proprietary Name buPROPion Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-450-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buPROPion Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110221
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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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