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Lunsumio

NDC 50242-159, Mosunetuzumab, concentrate, from Genentech, Inc..

Product NDC
50242-159
Status
Listed
Labeler
Genentech, Inc.
Dosage form
CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761263
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-159 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MOSUNETUZUMAB1 mg/mL
Package NDCNDC-11Package
50242-159-01502420159011 VIAL in 1 CARTON (50242-159-01) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ef0cf38-101c-4681-98fe-c05dc9ead443

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=50242-159

Use it

Look up 50242-159 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-159 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-159. 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.