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NDC 50242-127, Glofitamab, concentrate, from Genentech, Inc..

Product NDC
50242-127
Status
Listed
Labeler
Genentech, Inc.
Dosage form
CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761309
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLOFITAMAB10 mg/10mL

Pharmacologic classes

Bispecific CD20-directed CD3 T Cell Engager [EPC]; CD20-directed Antibody Interactions [MoA]; CD3 Receptor Agonists [MoA]; CD3-directed Antibody Interactions [MoA]; Cytochrome P450 Inhibitors [MoA]; Increased Cytokine Activity [PE]

Package NDCNDC-11Package
50242-127-01502420127011 VIAL, SINGLE-DOSE in 1 CARTON (50242-127-01) / 10 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3516e753-f064-4d30-9bd5-e3f2e143f75d

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=50242-127

Use it

Look up 50242-127 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-127. 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.