NDC 71335-9653 – Ropinirole
Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-9653
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA079229
- Marketed since
- September 15, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9653-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9653-1) | Mar 13, 2023 |
| 71335-9653-2 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9653-2) | Feb 14, 2023 |
| 71335-9653-3 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9653-3) | Nov 28, 2023 |
| 71335-9653-4 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9653-4) | Apr 3, 2024 |
| 71335-9653-5 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9653-5) | Jun 28, 2023 |
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