Ropinirole 68462-0254
Product NDC
68462-0254- 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
Need to source Ropinirole? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | .5 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (68462-254-01)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-254-10)
10 BLISTER PACK in 1 CARTON (68462-254-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK