# leflunomide

NDC: 71335-2832
Generic name: leflunomide
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091029

FDA application: ANDA077086

## Active ingredients

- LEFLUNOMIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa5f71b3-6a56-4616-baf7-4b761023b2a9
