# raloxifene hydrochloride

NDC: 68462-393
Generic name: raloxifene hydrochloride
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: 20160322

FDA application: ANDA204491

## 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:"68462-393"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-393
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c05521f8-95d2-44b8-8433-eba539c0f84c