Bupropion hydrochloride - Bupropion hydrochloride
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-736 |
| 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: | 100 |
| 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: |