NDC 43386-917
Potassium Chloride 20 meq tablet, extended release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Potassium Cation: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 20 meq
- Approval
- ANDA ANDA206347
- On the market since
- Jan 21, 2016
- Package NDCs
43386-917-0143386-917-0443386-917-0543386-917-0943386-917-10- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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