Ropinirole 46708-0265
Product NDC
46708-0265- Manufacturer
- Alembic Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 14, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA202786
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | 8 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(6)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-265-10)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-30)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-31)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-71)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-90)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-91)