# DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE

NDC: 0781-3493
Generic name: DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20200612

FDA application: ANDA209065

## 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:"0781-3493"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3493
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=809e8f77-390f-4cc8-8c8a-4f67a249c9df