# Dexmedetomidine Hydrochloride

NDC: 65219-642
Generic name: dexmedetomidine hydrochloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20150918

FDA application: ANDA201072

## Active ingredients

- DEXMEDETOMIDINE HYDROCHLORIDE: 100 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-642"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-642
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1896a96e-25f8-494e-9a96-6463b52fb102