Potassium Chloride 50090-7639
Product NDC
50090-7639- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 17, 1986
- Listing Expires
- December 31, 2026
- Application
- NDA019123
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Potassium Chloride | 750 mg/1 |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(4)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-0)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-1)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-2)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-3)