# Sotalol hydrochloride

NDC: 69724-112
Generic name: Sotalol hydrochloride
Labeler / Manufacturer: ALTATHERA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20151015

FDA application: NDA022306

## Active ingredients

- SOTALOL HYDROCHLORIDE: 15 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69724-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69724-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ff3061ab-d930-4318-a5be-684e38be229e
