Lutathera
NDC 69488-003, Lutetium Lu 177 dotatate, injection, from Advanced Accelerator Applications USA, Inc.
- Product NDC
- 69488-003
- Status
- Listed
- Labeler
- Advanced Accelerator Applications USA, Inc
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208700
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69488-003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LUTETIUM OXODOTREOTIDE LU-17710 mCi/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69488-003-01 | 69488000301 | 1 VIAL in 1 PACKAGE (69488-003-01) / 20.5 mL in 1 VIAL |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/72d1a024-00b7-418a-b36e-b2cb48f2ab55
Use it
Look up 69488-003 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69488-003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69488-003. 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.