NDC 71335-1231 – Ropinirole
Ropinirole Hydrochloride .25 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1231
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204022
- Marketed since
- October 17, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .25 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1231-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1231-1) | May 24, 2019 |
| 71335-1231-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1231-2) | Oct 31, 2024 |
| 71335-1231-3 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1231-3) | Oct 31, 2024 |
| 71335-1231-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1231-4) | Oct 31, 2024 |
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