NDC 43547-599 – Ropinirole hydrochloride
Ropinirole Hydrochloride 3 mg/1 · Tablet, Film Coated · Oral
Product NDC43547-599
Product details
- Brand name
- Ropinirole hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- SOLCO HEALTHCARE US, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078110
- Marketed since
- September 20, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 3 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 43547-599-10 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-599-10) | Sep 20, 2011 |
| 43547-599-50 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-599-50) | Sep 20, 2011 |
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