Ropinirole Hydrochloride 51655-0360
Product NDC
51655-0360- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA078110
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | .25 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(1)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-360-26)