NDC 50268-741 – Ropinirole hydrochloride
Ropinirole Hydrochloride .25 mg/1 · Tablet, Film Coated · Oral
Product NDC50268-741
Product details
- Brand name
- Ropinirole hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- AvPAK
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078110
- Marketed since
- August 19, 2022
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 50268-741-15 | 50 BLISTER PACK in 1 BOX (50268-741-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-741-11) | Aug 19, 2022 |
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