# OXYMORPHONE HYDROCHLORIDE

NDC: 72865-130
Generic name: OXYMORPHONE HYDROCHLORIDE
Labeler / Manufacturer: XLCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200506

FDA application: ANDA210175

## Active ingredients

- OXYMORPHONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72865-130"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72865-130
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a1d5061-b62a-49fa-a5b2-4970f51416ae