Ropinirole
NDC 69452-357, Ropinirole, tablet, film coated, from Bionpharma Inc..
- Product NDC
- 69452-357
- Status
- Listed
- Labeler
- Bionpharma Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA079229
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69452-357 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ROPINIROLE HYDROCHLORIDE.5 mg/1
Pharmacologic classes
Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69452-357-20 | 69452035720 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-357-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4e6b070c-50a6-4742-af3c-59b45c45735eNADAC price for package 69452035720
GET /v1/drugs/nadac/69452035720
Use it
Look up 69452-357 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69452-357 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69452-357. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.