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NDC 70255-010, BINIMETINIB, tablet, film coated, from Array BioPharma Inc..

Product NDC
70255-010
Status
Listed
Labeler
Array BioPharma Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA210498
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70255-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BINIMETINIB15 mg/1
Package NDCNDC-11Package
70255-010-02702550010021 BOTTLE in 1 CARTON (70255-010-02) / 180 TABLET, FILM COATED in 1 BOTTLE
70255-010-037025500100390 TABLET, FILM COATED in 1 BOTTLE (70255-010-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6c3408ac-d401-4925-8a03-26591afbc240

Use it

Look up 70255-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70255-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70255-010. 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.