# OXYMORPHONE HYDROCHLORIDE

NDC: 31722-929
Generic name: OXYMORPHONE HYDROCHLORIDE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180301

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:"31722-929"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-929
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06af7dff-c261-4c03-9cd9-0605c42507fa