# Dexmedetomidine Hydrochloride

NDC: 63323-671
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: 20190513

FDA application: ANDA208129

## Active ingredients

- DEXMEDETOMIDINE HYDROCHLORIDE: 4 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-671"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-671
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d5d2294-89a0-4b6f-aa00-d39a0393b6a8