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POLIVY

NDC 50242-105, polatuzumab vedotin, injection, powder, lyophilized, for solution, from Genentech, Inc..

Product NDC
50242-105
Status
Listed
Labeler
Genentech, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761121
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POLATUZUMAB VEDOTIN140 mg/7.52mL
Package NDCNDC-11Package
50242-105-01502420105011 VIAL, SINGLE-DOSE in 1 CARTON (50242-105-01) / 20 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/20a16ab2-f338-4abb-9dcd-254bd949a2bc

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=50242-105

Use it

Look up 50242-105 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-105. 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.