HUMATROPE
NDC 0002-8147, Somatropin, kit, from Eli Lilly and Company.
- Product NDC
- 0002-8147
- Status
- Listed
- Labeler
- Eli Lilly and Company
- Dosage form
- KIT
- Route
- INTRAMUSCULAR, SUBCUTANEOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- BLA
- Application
- BLA019640
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0002-8147 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0002-8147-01 | 00002814701 | 1 TRAY in 1 CARTON (0002-8147-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a774e1ae-3997-49ee-8b0e-99a2b315d409
Use it
Look up 0002-8147 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0002-8147 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0002-8147. 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.