Ropinirole 68462-0257
Product NDC
68462-0257- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 25, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA090135
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | 3 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (68462-257-01)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-257-10)