Rufinamide
NDC 31722-599, Rufinamide, tablet, film coated, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-599
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204993
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/31722-599 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- RUFINAMIDE400 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 31722-599-12 | 31722059912 | 120 TABLET, FILM COATED in 1 BOTTLE (31722-599-12) |
| 31722-599-30 | 31722059930 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-599-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/afe24968-e078-46d6-a776-b2608734e03eNADAC price for package 31722059912
GET /v1/drugs/nadac/31722059912
Use it
Look up 31722-599 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-599 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-599. 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.