# Raloxifene Hydrochloride

NDC: 76282-256
Generic name: Raloxifene Hydrochloride
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20141112

FDA application: ANDA090842

## 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:"76282-256"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-256
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b94ecf5-d870-4132-b455-d5ee5c9dce56