NDC Code | 0591-3612-19 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3612-19) |
Product NDC | 0591-3612 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ropinirole Hydrochloride |
Non-Proprietary Name | Ropinirole Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20120606 |
Marketing Category Name | ANDA |
Application Number | ANDA200431 |
Manufacturer | Watson Laboratories, Inc. |
Substance Name | ROPINIROLE HYDROCHLORIDE |
Strength | 12 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |