Ropinirole
- Product NDC
- 72162-2200
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ropinirole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079229
- Marketing category
- ANDA
- Substance
- ROPINIROLE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2200-1 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2200-1) | 2023-12-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ropinirole | Bryant Ranch Prepack | 2023-12-15 | HUMAN PRESCRIPTION DRUG LABEL | 100 |