Ropinirole Hydrochloride - Ropinirole Hydrochloride
Navigation: NDC > Supplier starting with: T > TEVA PHARMACEUTICALS USA INC| Field | Value |
|---|---|
| NDC Code: | 0093-5285 |
| Proprietary Name: | Ropinirole Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Ropinirole Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 07-05-2008 |
| End of Marketing: | 31-05-2014 |
| Category Name: | ANDA |
| Application Number: | ANDA077460 |
| Labeler: | TEVA PHARMACEUTICALS USA INC |
| Substance Name: | ROPINIROLE HYDROCHLORIDE |
| Active Numerator Strength: | 2 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
| DEA Schedule: |