# DEXMEDETOMIDINE HYDROCHLORIDE

NDC: 43066-565
Generic name: DEXMEDETOMIDINE HYDROCHLORIDE
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20190827

FDA application: ANDA208532

## 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:"43066-565"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-565
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32242f34-6e2b-4098-bd8e-3d55162f31b5