Drugplain

NDC 83107-010-60

BETAPACE AF 160 mg/1

sotalol hydrochloride · TABLET

No Recall History

BETAPACE AF is a tablet containing sotalol hydrochloride at a strength of 160 mg/1. Manufactured by Legacy Pharma USA, Inc..

Key Facts

Brand Name
BETAPACE AF
Generic Name
sotalol hydrochloride
NDC Code (Package)
83107-010-60
NDC Code (Product)
83107-010
Manufacturer
Legacy Pharma USA, Inc.
Strength
160 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
NDA019865
Marketing Start
09/01/2016

Recall History

No Recall History

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BETAPACE AF — All Packages

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.