# teriflunomide

NDC: 68462-424
Generic name: teriflunomide
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230119

FDA application: ANDA209663

## Active ingredients

- TERIFLUNOMIDE: 14 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-424"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-424
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb431ea0-ba0f-4b5d-a50d-f8c050762242