# Sotalol Hydrochloride

NDC: 69584-844
Generic name: Sotalol Hydrochloride
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200724

FDA application: ANDA075563

## Active ingredients

- SOTALOL HYDROCHLORIDE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69584-844"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-844
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8ac6351-b1e9-4dd2-82f2-5980814fda15