Quick answers
- What is POKONZA potassium chloride?
- POKONZA potassium chloride is a brand name of Potassium chloride, a prescription medicine. The FDA NDC Directory lists 1 POKONZA potassium chloride product in 1 strength and form.
- Who makes POKONZA potassium chloride?
- Genus Lifesciences holds the FDA application for POKONZA potassium chloride (NDA206814, approved December 22, 2014).
- Is there a generic or store brand of POKONZA potassium chloride?
- Other products of Potassium chloride are listed with the FDA, but none in exactly the same strength and form as a POKONZA potassium chloride product.
- Has POKONZA potassium chloride been recalled?
- No recall linked to POKONZA potassium chloride products (by their NDC code or label) appears in the FDA enforcement reports we use.
What POKONZA potassium chloride is
Each POKONZA potassium chloride product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Potassium chloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| potassium chloride 10 meq/15 mL liquid (oral) | POKONZA potassium chloride | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Potassium chloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA206814 | Genus Lifesciences | December 22, 2014 | 1 |
Companies that list POKONZA potassium chloride
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of POKONZA potassium chloride products.
Recalls
No recall linked to POKONZA potassium chloride products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.