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Hemlibra

NDC 50242-930, emicizumab, injection, solution, from Genentech, Inc..

Product NDC
50242-930
Status
Listed
Labeler
Genentech, Inc.
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761083
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-930 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EMICIZUMAB300 mg/2mL
Package NDCNDC-11Package
50242-930-01502420930011 VIAL, SINGLE-USE in 1 CARTON (50242-930-01) / 2 mL in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2483adba-fab6-4d1b-96c5-c195577ed071

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=50242-930

Use it

Look up 50242-930 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-930 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-930. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.