NDC 42291-507

Potassium Chloride 1500 mg tablet, extended release

On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-5325.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it and packages it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Product details

Generic drug
Potassium Cation: every company that makes it
Form
tablet, extended release, oral
Strength
1500 mg
Approval
ANDA ANDA074726
On the market since
Jun 19, 2019
Package NDCs
42291-507-01 42291-507-50
Official label
DailyMed (National Library of Medicine), updated Jul 23, 2025

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