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Warfarin Sodium

NDC 51672-4035, Warfarin Sodium, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4035
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040301
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4035 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • WARFARIN SODIUM10 mg/1

Pharmacologic classes

Vitamin K Antagonist [EPC]; Vitamin K Inhibitors [MoA]

Package NDCNDC-11Package
51672-4035-151672403501100 TABLET in 1 BOTTLE (51672-4035-1)
51672-4035-3516724035031000 TABLET in 1 BOTTLE (51672-4035-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8ad881e0-ca41-42ad-9d7d-eb85b3a30af0

  • NADAC price for package 51672403501

    GET /v1/drugs/nadac/51672403501

  • NADAC price for package 51672403503

    GET /v1/drugs/nadac/51672403503

Use it

Look up 51672-4035 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4035 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4035. 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.