# Esmolol Hydrochloride

NDC: 10019-120
Generic name: Esmolol Hydrochloride
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19861231

FDA application: NDA019386

## Active ingredients

- ESMOLOL HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10019-120"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10019-120
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0a56c07-8f0f-4499-8d00-f13a966bf988