NDC 0121-1896
Potassium Chloride 20 meq per 30 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it, tests it, packages it and labels it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Product details
- Generic drug
- Potassium Cation: every company that makes it
- Form
- solution, oral
- Strength
- 20 meq per 30 mL
- Approval
- ANDA ANDA210766
- On the market since
- Mar 27, 2023
- Package NDCs
0121-1896-000121-1896-300121-1896-400121-1896-50- Official label
- DailyMed (National Library of Medicine), updated Nov 19, 2024
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