NDC 71335-1626 – Ropinirole hydrochloride
Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1626
Product details
- Brand name
- Ropinirole hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078110
- Marketed since
- September 20, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 2 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1626-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1626-1) | Jun 8, 2020 |
| 71335-1626-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1626-2) | Jun 8, 2020 |
| 71335-1626-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1626-3) | Jun 8, 2020 |
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