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Sunitinib Malate

NDC 0093-8199, Sunitinib Malate, capsule, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-8199
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213803
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8199 \
  -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
0093-8199-280009381992828 CAPSULE in 1 BOTTLE (0093-8199-28)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9479e5f-914f-46ca-95c1-327c66457e47

Use it

Look up 0093-8199 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8199 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-8199. 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.