Ropinirole 72189-0222
Product NDC
72189-0222- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 20, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA204022
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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)
30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)