# SOTALOL HYDROCHLORIDE

NDC: 11788-052
Generic name: SOTALOL HYDROCHLORIDE
Labeler / Manufacturer: AiPing Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251101

FDA application: ANDA075500

## 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:"11788-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11788-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56326224-fc80-4b89-8ba3-70cb873173b4