# Oxymorphone Hydrochloride

NDC: 10702-071
Generic name: Oxymorphone Hydrochloride
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130211

FDA application: ANDA203601

## Active ingredients

- OXYMORPHONE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10702-071"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-071
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dcb5b5d2-7d0a-497a-8f1e-3b96fd43320b