# Hydromorphone Hydrochloride

NDC: 63323-853
Generic name: Hydromorphone Hydrochloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20171215

FDA application: NDA019034

## Active ingredients

- HYDROMORPHONE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e034eb96-03e0-46e1-8b92-5e1f94555e7b