# Sotalol Hydrochloride

NDC: 72162-1932
Generic name: Sotalol Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
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: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1932"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1932
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0fd4afc7-dbf8-46be-9657-aa83bbb2c026