Details for New Drug Application (NDA): 218733
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The generic ingredient in POTASSIUM CHLORIDE is calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate. There are two hundred and eighty-two drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate profile page.
Summary for 218733
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Macleods Pharms Ltd |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 218733
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 218733
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | SOLUTION;ORAL | 218733 | ANDA | Macleods Pharmaceuticals Limited | 33342-511 | 33342-511-73 | 473 mL in 1 BOTTLE (33342-511-73) |
| POTASSIUM CHLORIDE | potassium chloride | SOLUTION;ORAL | 218733 | ANDA | Macleods Pharmaceuticals Limited | 33342-512 | 33342-512-73 | 473 mL in 1 BOTTLE (33342-512-73) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 20MEQ/15ML | ||||
| Approval Date: | Sep 10, 2025 | TE: | AA | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 40MEQ/15ML | ||||
| Approval Date: | Sep 10, 2025 | TE: | AA | RLD: | No | ||||
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