NDC 72789-135

Sotalol Hydrochloride 160 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-843.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Repackaging site

Product details

Generic drug
Sotalol: every company that makes it
Form
tablet, oral
Strength
160 mg
Approval
ANDA ANDA075563
On the market since
Jul 24, 2020
Package NDCs
72789-135-01
Official label
DailyMed (National Library of Medicine), updated Oct 15, 2026

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