# Dexmedetomidine Hydrochloride

NDC: 68083-239
Generic name: Dexmedetomidine Hydrochloride
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20200603

FDA application: ANDA209307

## 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:"68083-239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f307de7e-a9ab-4734-abb7-66b4e112bc51