# DEXMEDETOMIDINE HYDROCHLORIDE

NDC: 67457-925
Generic name: DEXMEDETOMIDINE HYDROCHLORIDE
Labeler / Manufacturer: Mylan Institutional LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20201113

FDA application: ANDA212571

## Active ingredients

- DEXMEDETOMIDINE HYDROCHLORIDE: 400 ug/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67457-925"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67457-925
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f140de5a-f13d-46b4-a742-049c63e474f5