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Rituxan

NDC 50242-051, rituximab, injection, solution, from Genentech, Inc..

Product NDC
50242-051
Status
Listed
Labeler
Genentech, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA103705
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-051 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RITUXIMAB10 mg/mL

Pharmacologic classes

CD20-directed Antibody Interactions [MoA]; CD20-directed Cytolytic Antibody [EPC]

Package NDCNDC-11Package
50242-051-21502420051211 VIAL, SINGLE-USE in 1 CARTON (50242-051-21) / 10 mL in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b172773b-3905-4a1c-ad95-bab4b6126563

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=50242-051

Use it

Look up 50242-051 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-051 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-051. 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.