TAVALISSE
NDC 71332-002, FOSTAMATINIB, tablet, from Rigel Pharmaceuticals, Inc..
- Product NDC
- 71332-002
- Status
- Listed
- Labeler
- Rigel Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA209299
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71332-002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FOSTAMATINIB150 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71332-002-01 | 71332000201 | 60 TABLET in 1 BOTTLE (71332-002-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/21149cc3-049b-43e2-b141-c9499160556c
Use it
Look up 71332-002 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71332-002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71332-002. 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.