Dimethyl Fumarate
NDC 43598-430, Dimethyl fumarate, capsule, delayed release, from Dr. Reddy's Laboratories Inc..
- Product NDC
- 43598-430
- Status
- Listed
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210460
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43598-430 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIMETHYL FUMARATE240 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43598-430-60 | 43598043060 | 1 BOTTLE in 1 CARTON (43598-430-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b00dcf89-59d3-9ab2-fd9b-16b9ec2d677bNADAC price for package 43598043060
GET /v1/drugs/nadac/43598043060
Use it
Look up 43598-430 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43598-430 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43598-430. 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.