# Hydromorphone Hydrochloride

NDC: 0409-3365
Generic name: HYDROMORPHONE HYDROCHLORIDE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20111201

FDA application: NDA200403

## 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:"0409-3365"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-3365
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9c9ef18-7dfc-4322-b2fc-29b934c30f8b