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Sunitinib malate

NDC 63304-091, Sunitinib malate, capsule, from Sun Pharmaceutical Industries Inc..

Product NDC
63304-091
Status
Listed
Labeler
Sun Pharmaceutical Industries Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213914
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUNITINIB MALATE12.5 mg/1

Pharmacologic classes

Kinase Inhibitor [EPC]; Protein Kinase Inhibitors [MoA]

Package NDCNDC-11Package
63304-091-276330400912728 CAPSULE in 1 BOTTLE (63304-091-27)
63304-091-86633040091864 BLISTER PACK in 1 BOX (63304-091-86) / 7 CAPSULE in 1 BLISTER PACK (63304-091-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06e0ad28-6637-4f54-879c-2c194aece5fd

Use it

Look up 63304-091 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-091. 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.