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Bupropion Hydrochloride - Bupropion Hydrochloride

Navigation: NDC > Supplier starting with: S > SANDOZ INC
Field Value
NDC Code: 0781-5169
Proprietary Name: Bupropion Hydrochloride
Suffix:
Non-Proprietary Name: Bupropion Hydrochloride
Dosage Form: TABLET, EXTENDED RELEASE
Method: ORAL
Original Marketing Date: 12-03-2008
Category Name: ANDA
Application Number: ANDA077475
Labeler: SANDOZ INC
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: