NDC 60687-577 – Ropinirole hydrochloride
Ropinirole Hydrochloride .25 mg/1 · Tablet, Film Coated · Oral
Product NDC60687-577
Product details
- Brand name
- Ropinirole hydrochloride
- Generic name
- Ropinirole hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078110
- Marketed since
- June 10, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .25 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-577-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-577-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-577-11) | Jun 10, 2021 |
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