BUPROPION HYDROCHLORIDE - bupropion hydrochloride
Navigation: NDC > Supplier starting with: P > PAR PHARMACEUTICAL, INC.| Field | Value |
|---|---|
| NDC Code: | 10370-101 |
| Proprietary Name: | BUPROPION HYDROCHLORIDE |
| Suffix: | |
| Non-Proprietary Name: | bupropion hydrochloride |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 25-11-2008 |
| Category Name: | ANDA |
| Application Number: | ANDA077284 |
| Labeler: | PAR PHARMACEUTICAL, 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: |