NDC 71335-0829 – Ropinirole Hydrochloride
Ropinirole Hydrochloride 1 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0829
Product details
- Brand name
- Ropinirole Hydrochloride
- Generic name
- Ropinirole Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090429
- Marketed since
- January 29, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 1 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0829-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0829-1) | May 15, 2018 |
| 71335-0829-2 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0829-2) | Jan 29, 2025 |
| 71335-0829-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0829-3) | Jan 29, 2025 |
| 71335-0829-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0829-4) | Jan 29, 2025 |
| 71335-0829-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0829-5) | Jan 29, 2025 |
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