NDC 42291-506
Potassium Chloride 750 mg tablet, film coated, extended release
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-5323.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
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
- Jun 21, 2019
- Package NDCs
42291-506-0142291-506-50- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2025
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