# DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE

NDC: 43066-555
Generic name: DEXMEDETOMIDINE HYDROCHLORIDE in 0.9% sodium chloride
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: 200 ug/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43066-555"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-555
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aea9a3ad-c244-42be-9cd3-5df83fe2b522