Ropinirole Hydrochloride 43547-0270
Product NDC
43547-0270- Manufacturer
- Solco Healthcare Us, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 20, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA078110
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | 1 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-270-10)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-270-50)