Bupropion Hydrocloride - Bupropion Hydrochloride
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NDC Code: | 49349-230 |
Proprietary Name: | Bupropion Hydrocloride |
Suffix: | |
Non-Proprietary Name: | Bupropion Hydrochloride |
Dosage Form: | TABLET, FILM COATED |
Method: | ORAL |
Original Marketing Date: | 14-03-2011 |
Category Name: | ANDA |
Application Number: | ANDA075584 |
Labeler: | REMEDYREPACK INC. |
Substance Name: | BUPROPION HYDROCHLORIDE |
Active Numerator Strength: | 75 |
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: |