DIMETHYL FUMARATE
NDC 31722-680, dimethyl fumarate, kit, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-680
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210500
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/31722-680 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 31722-680-60 | 31722068060 | 1 KIT in 1 KIT (31722-680-60) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b856ac70-71cd-477b-95b1-0a6132c260e8
Use it
Look up 31722-680 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-680 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-680. 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.