# Dexmedetomidine Hydrochloride in Sodium Chloride

NDC: 68094-047
Generic name: Dexmedetomidine Hydrochloride
Labeler / Manufacturer: Precision Dose, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20201123

FDA application: ANDA212857

## 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:"68094-047"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68094-047
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9d5c989-ebf6-4377-9c6e-7aef848a03a1