NDC 42291-714 – Ropinirole Hydrochloride
Ropinirole Hydrochloride 4 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC42291-714
Product details
- Brand name
- Ropinirole Hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- AvKARE
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090869
- Marketed since
- September 13, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42291-714-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-714-30) | Nov 1, 2023 |
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