DIMETHYL FUMARATE
NDC 69097-323, DIMETHYL FUMARATE, capsule, delayed release, from Cipla USA Inc..
- Product NDC
- 69097-323
- Status
- Listed
- Labeler
- Cipla USA Inc.
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210305
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69097-323 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIMETHYL FUMARATE240 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69097-323-03 | 69097032303 | 1 BOTTLE, PLASTIC in 1 CARTON (69097-323-03) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/6c42107a-2a42-4263-97b6-ae0d7675c92aNADAC price for package 69097032303
GET /v1/drugs/nadac/69097032303
Use it
Look up 69097-323 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69097-323 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69097-323. 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.