Ropinirole 55111-0661
Product NDC
55111-0661- Manufacturer
- Dr. Reddys Laboratories Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 6, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA201576
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | 4 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(3)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-05)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-30)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-90)