# Hydromorphone Hydrochloride

NDC: 0641-6169
Generic name: Hydromorphone Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20240426

FDA application: ANDA216899

## 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:"0641-6169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31d5a37a-0e90-4e88-be14-75c877be9de2