# Raloxifene hydrochloride

NDC: 72241-010
Generic name: Raloxifene hydrochloride
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20171230

FDA application: ANDA211324

## Active ingredients

- RALOXIFENE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0db29f5-28da-4165-94f8-24727b6b71e5