NDC 10702-014

Betaxolol Hydrochloride 20 mg tablet, coated

On the label: KVK-TECH, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Betaxolol: every company that makes it
Form
tablet, coated, oral
Strength
20 mg
Approval
ANDA ANDA078962
On the market since
Nov 2, 2011
Package NDCs
10702-014-01
Official label
DailyMed (National Library of Medicine), updated Apr 30, 2024

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