NDC 0228-3658 – Ropinirole
Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0228-3658
Product details
- Brand name
- Ropinirole
- Generic name
- Ropinirole
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090869
- Marketed since
- August 23, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 2 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0228-3658-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3658-03) | Aug 23, 2012 |
| 0228-3658-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3658-09) | Aug 23, 2012 |
Other Ropinirole products
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- 0228-3660 Ropinirole Hydrochloride 8 mg/1 · Tablet, Film Coated, Extended Release · Actavis Pharma, Inc.
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