# Hydromorphone Hydrochloride

NDC: 60760-998
Generic name: Hydromorphone Hydrochloride
Labeler / Manufacturer: St. Mary's Medical Park Pharmacy
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: NDA AUTHORIZED GENERIC
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260609

FDA application: NDA019892

## Active ingredients

- HYDROMORPHONE HYDROCHLORIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-998"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-998
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=53ddcacc-99e4-8b21-e063-6394a90a3e79