# DEXMEDETOMIDINE

NDC: 71288-505
Generic name: DEXMEDETOMIDINE
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190118

FDA application: ANDA204843

## Active ingredients

- DEXMEDETOMIDINE HYDROCHLORIDE: 100 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-505"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-505
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8fa36783-b94d-4084-8c41-40ee64192074