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Bupropion hydrochloride - Bupropion hydrochloride

Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE
Field Value
NDC Code: 47335-737
Proprietary Name: Bupropion hydrochloride
Suffix:
Non-Proprietary Name: Bupropion hydrochloride
Dosage Form: TABLET, FILM COATED, EXTENDED RELEASE
Method: ORAL
Original Marketing Date: 08-04-2010
Category Name: ANDA
Application Number: ANDA078866
Labeler: SUN PHARMA GLOBAL FZE
Substance Name: BUPROPION HYDROCHLORIDE
Active Numerator Strength: 150
Active Ingredient Unit: mg/1
Pharm Classes: Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
DEA Schedule: