# SOTYLIZE

NDC: 24338-530
Generic name: SOTALOL HYDROCHLORIDE
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20150301

FDA application: NDA205108

## Active ingredients

- SOTALOL HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f33f900-0777-4a92-a7f7-00cf3d57d95c