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NDC 50242-717, COBIMETINIB, tablet, film coated, from Genentech, Inc..

Product NDC
50242-717
Status
Listed
Labeler
Genentech, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA206192
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50242-717 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • COBIMETINIB FUMARATE20 mg/1

Pharmacologic classes

Kinase Inhibitor [EPC]; Kinase Inhibitors [MoA]

Package NDCNDC-11Package
50242-717-015024207170163 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50242-717-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c387579e-cee0-4334-bd1e-73f93ac1bde6

Use it

Look up 50242-717 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50242-717 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50242-717. 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.