Potassium Chloride 71656-0021
Generic: Potassium Chloride Oral
Product NDC
71656-0021- Manufacturer
- Saptalis Pharmaceuticals, Llc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 5, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA211648
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Potassium Chloride | 1.5 g/15mL |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(5)
10 TRAY in 1 CASE (71656-021-01) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)
10 TRAY in 1 CASE (71656-021-02) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)
473 mL in 1 BOTTLE (71656-021-16)
5 TRAY in 1 CASE (71656-021-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)
5 TRAY in 1 CASE (71656-021-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)