NDC 55111-659 – Ropinirole
Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC55111-659
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Dr. Reddys Laboratories Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA201576
- Marketed since
- June 6, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 2 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 55111-659-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-05) | Jun 6, 2012 |
| 55111-659-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-30) | Jun 6, 2012 |
| 55111-659-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-90) | Jun 6, 2012 |
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