# Hydromorphone Hydrochloride

NDC: 0054-0386
Generic name: hydromorphone hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20120301

FDA application: ANDA074653

## Active ingredients

- HYDROMORPHONE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0386"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0386
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc574063-6ede-4da7-82c4-7450c92b229b