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NDC 0002-7722, mirikizumab-mrkz, kit, from Eli Lilly and Company.

Product NDC
0002-7722
Status
Listed
Labeler
Eli Lilly and Company
Dosage form
KIT
Route
SUBCUTANEOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761279
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0002-7722 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
0002-7722-11000027722111 KIT in 1 CARTON (0002-7722-11) * 1 mL in 1 SYRINGE (0002-8870-01) * 2 mL in 1 SYRINGE (0002-1442-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/472cbe04-263e-433d-9a0f-58c1b50b715a
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0002-7722

Use it

Look up 0002-7722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0002-7722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0002-7722. 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.