# Dexmedetomidine

NDC: 83634-600
Generic name: dexmedetomidine
Labeler / Manufacturer: Avenacy Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20240315

FDA application: ANDA209065

## 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:"83634-600"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83634-600
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eee6145b-d83f-4596-92d3-733934d8a3a4