Ropinirole
NDC 70518-4318, Ropinirole, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-4318
- Status
- Listed
- Labeler
- REMEDYREPACK 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/70518-4318 \ -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 |
|---|---|---|
| 70518-4318-0 | 70518431800 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4318-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cdc63b7a-062a-4519-a63e-e48a356f641c
Use it
Look up 70518-4318 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4318 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4318. 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.