Dimethyl Fumarate
NDC 69238-1319, Dimethyl Fumarate, capsule, delayed release, from Amneal Pharmaceuticals NY LLC.
- Product NDC
- 69238-1319
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals NY LLC
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210402
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1319 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIMETHYL FUMARATE240 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69238-1319-6 | 69238131906 | 1 BOTTLE in 1 CARTON (69238-1319-6) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4c7626c6-2b1b-4865-818c-0c79c18c049dNADAC price for package 69238131906
GET /v1/drugs/nadac/69238131906
Use it
Look up 69238-1319 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1319 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69238-1319. 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.