Ropinirole Hydrochloride - Ropinirole Hydrochloride
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-3612 |
| Proprietary Name: | Ropinirole Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Ropinirole Hydrochloride |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 06-06-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA200431 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | ROPINIROLE HYDROCHLORIDE |
| Active Numerator Strength: | 12 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
| DEA Schedule: |