NDC 51655-360 – Ropinirole hydrochloride
Ropinirole Hydrochloride .25 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-360
Product details
- Brand name
- Ropinirole hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078110
- Marketed since
- May 28, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .25 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-360-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-360-26) | May 28, 2020 |
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