# DEXMEDETOMIDINE HYDROCHLORIDE

NDC: 71225-126
Generic name: dexmedetomidine hydrochloride
Labeler / Manufacturer: Slayback Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20191206
Marketing ended: 20260731
FDA application: ANDA212791

## Active ingredients

- DEXMEDETOMIDINE HYDROCHLORIDE: 4 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71225-126"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71225-126
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5d28ed8-e427-4850-81aa-98702d3b6a5d