NDC 0615-8189 – Ropinirole Hydrochloride
Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Oral
Product NDC0615-8189
Product details
- Brand name
- Ropinirole Hydrochloride
- Generic name
- Ropinirole Hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090429
- Marketed since
- January 29, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonergot Dopamine Agonist
Active ingredients
- Ropinirole Hydrochloride .5 mg/1
Uses, dosage, side effects and warnings for Ropinirole hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8189-39 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8189-39) | Mar 6, 2018 |
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