# Leflunomide

NDC: 68071-3763
Generic name: Leflunomide
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200831

FDA application: ANDA211863

## Active ingredients

- LEFLUNOMIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3763"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3763
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b5c98d0-de59-85f6-e063-6394a90ab67a