DIMETHYL FUMARATE
NDC 82009-138, DIMETHYL FUMARATE, capsule, delayed release, from Quallent Pharmaceuticals Health LLC.
- Product NDC
- 82009-138
- Status
- Listed
- Labeler
- Quallent Pharmaceuticals Health LLC
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210500
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82009-138 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIMETHYL FUMARATE240 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82009-138-60 | 82009013860 | 1 BOTTLE in 1 CARTON (82009-138-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/39150ef0-ba48-4719-b7fd-9beb4d4ad3ceNADAC price for package 82009013860
GET /v1/drugs/nadac/82009013860
Use it
Look up 82009-138 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82009-138 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82009-138. 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.