# Mifepristone

NDC: 84670-014
Generic name: MIFEPRISTONE
Labeler / Manufacturer: Evita Solutions LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250930

FDA application: ANDA216616

## Active ingredients

- MIFEPRISTONE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84670-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84670-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=839d7a7d-de19-42bd-8810-132b3c2a5daf