NDC 51655-226

Potassium Chloride 750 mg tablet, film coated, extended release

On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-5323.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Potassium Cation: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
750 mg
Approval
NDA NDA019123
On the market since
Oct 25, 2022
Package NDCs
51655-226-26 51655-226-52
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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