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Rivaroxaban

NDC 51672-4228, Rivaroxaban, tablet, coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4228
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208557
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4228 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RIVAROXABAN2.5 mg/1

Pharmacologic classes

Factor Xa Inhibitor [EPC]; Factor Xa Inhibitors [MoA]

Package NDCNDC-11Package
51672-4228-45167242280460 TABLET, COATED in 1 BOTTLE (51672-4228-4)
51672-4228-951672422809180 TABLET, COATED in 1 BOTTLE (51672-4228-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/925a9a11-ae5b-405c-96d2-b1be4b85bf71

  • NADAC price for package 51672422804

    GET /v1/drugs/nadac/51672422804

  • NADAC price for package 51672422809

    GET /v1/drugs/nadac/51672422809

Use it

Look up 51672-4228 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4228 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4228. 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.