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NDC 50242-090, Vemurafenib, tablet, film coated, from Genentech, Inc..

Product NDC
50242-090
Status
Listed
Labeler
Genentech, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA202429
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VEMURAFENIB240 mg/1

Pharmacologic classes

Cytochrome P450 1A2 Inhibitors [MoA]; Kinase Inhibitor [EPC]; P-Glycoprotein Inhibitors [MoA]; Protein Kinase Inhibitors [MoA]

Package NDCNDC-11Package
50242-090-02502420090021 BOTTLE, PLASTIC in 1 CARTON (50242-090-02) / 112 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/38eea320-7e0c-485a-bc30-98c3c45e2763

Use it

Look up 50242-090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-090. 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.