DIMETHYL FUMARATE
NDC 69097-552, DIMETHYL FUMARATE, kit, from Cipla USA Inc..
- Product NDC
- 69097-552
- Status
- Listed
- Labeler
- Cipla USA Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210305
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69097-552 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69097-552-03 | 69097055203 | 1 KIT in 1 KIT (69097-552-03) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 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-ae0d7675c92a
Use it
Look up 69097-552 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69097-552 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69097-552. 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.