# Dexmedetomidine Hydrochloride

NDC: 57664-596
Generic name: DEXMEDETOMIDINE HYDROCHLORIDE
Labeler / Manufacturer: Sun Pharmaceuticals Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20150408

FDA application: ANDA202126

## 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:"57664-596"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-596
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fe788bc-4ad1-4b32-83d3-dcbfcd8429aa