Armodafinil
NDC 0093-3090, Armodafinil, tablet, from Teva Pharmaceuticals USA, Inc..
- Product NDC
- 0093-3090
- Status
- Listed
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA021875
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/0093-3090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ARMODAFINIL50 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0093-3090-56 | 00093309056 | 30 TABLET in 1 BOTTLE (0093-3090-56) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b3cac300-c3d2-4189-a410-2aaf3773c090NADAC price for package 00093309056
GET /v1/drugs/nadac/00093309056
Use it
Look up 0093-3090 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0093-3090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0093-3090. 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.