Ropinirole 69452-0359
Product NDC
69452-0359- Manufacturer
- Bionpharma Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 15, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA079229
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ropinirole Hydrochloride | 2 mg/1 |
Drug Class
Dopamine Agonists [MoA]Nonergot Dopamine Agonist [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-359-20)