Budeprion - 63629-3762-2 - (Bupropion Hydrochloride)

Alphabetical Index


Drug Information of Budeprion

Product NDC: 63629-3762
Proprietary Name: Budeprion
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Bupropion Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Budeprion

Product NDC: 63629-3762
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077284
Marketing Category: ANDA
Start Marketing Date: 20080530

Package Information of Budeprion

Package NDC: 63629-3762-2
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3762-2)

NDC Information of Budeprion

NDC Code 63629-3762-2
Proprietary Name Budeprion
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3762-2)
Product NDC 63629-3762
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080530
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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 Budeprion


General Information