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leflunomide

NDC 70710-1158, leflunomide, tablet, film coated, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1158
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212308
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1158 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEFLUNOMIDE20 mg/1

Pharmacologic classes

Antirheumatic Agent [EPC]

Package NDCNDC-11Package
70710-1158-170710115801100 TABLET, FILM COATED in 1 BOTTLE (70710-1158-1)
70710-1158-37071011580330 TABLET, FILM COATED in 1 BOTTLE (70710-1158-3)
70710-1158-570710115805500 TABLET, FILM COATED in 1 BOTTLE (70710-1158-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b9af9870-014f-4c4e-8738-bb04b30b3e85

  • NADAC price for package 70710115803

    GET /v1/drugs/nadac/70710115803

Use it

Look up 70710-1158 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1158 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1158. 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.