# Dexmedetomidine Hydrochloride

NDC: 70069-759
Generic name: Dexmedetomidine Hydrochloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240926

FDA application: ANDA218112

## 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:"70069-759"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-759
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=649e777b-9b30-4f1e-9fb9-6bba57580976