# Dexmedetomidine

NDC: 16729-239
Generic name: Dexmedetomidine
Labeler / Manufacturer: Accord Healthcare Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20161221

FDA application: ANDA204023

## 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:"16729-239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16729-239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b9881f0-4a66-660f-e054-00144ff88e88