# Esmolol Hydrochloride

NDC: 63323-652
Generic name: ESMOLOL HYDROCHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20041130

FDA application: ANDA076573

## Active ingredients

- ESMOLOL HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-652"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-652
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fdc9cea8-0eb4-4930-9e1c-d44bfa9346d2