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sorafenib

NDC 24979-715, sorafenib, tablet, film coated, from Upsher-Smith Laboratories, LLC.

Product NDC
24979-715
Status
Listed
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209050
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24979-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SORAFENIB200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
24979-715-042497907150460 TABLET, FILM COATED in 1 BOTTLE (24979-715-04)
24979-715-4424979071544120 TABLET, FILM COATED in 1 BOTTLE (24979-715-44)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68aa4b7f-3f13-4e73-b572-aa6c11a8429c

Use it

Look up 24979-715 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24979-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24979-715. 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.