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Alunbrig

NDC 63020-090, brigatinib, tablet, film coated, from Takeda Pharmaceuticals America, Inc..

Product NDC
63020-090
Status
Listed
Labeler
Takeda Pharmaceuticals America, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA208772
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63020-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BRIGATINIB90 mg/1

Pharmacologic classes

Cytochrome P450 3A Inducers [MoA]; Kinase Inhibitor [EPC]; Tyrosine Kinase Inhibitors [MoA]

Package NDCNDC-11Package
63020-090-07630200090077 TABLET, FILM COATED in 1 BOTTLE (63020-090-07)
63020-090-306302000903030 TABLET, FILM COATED in 1 BOTTLE (63020-090-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0fe9ff20-d402-41f3-bc1e-7002ea7007db

Use it

Look up 63020-090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63020-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63020-090. 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.