Details for New Drug Application (NDA): 217704
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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 217704
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Nexus |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 217704
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 217704
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | INJECTABLE;INJECTION | 217704 | ANDA | Nexus Pharmaceuticals LLC | 14789-136 | 14789-136-05 | 25 VIAL, GLASS in 1 CARTON (14789-136-05) / 10 mL in 1 VIAL, GLASS (14789-136-07) |
| POTASSIUM CHLORIDE | potassium chloride | INJECTABLE;INJECTION | 217704 | ANDA | Nexus Pharmaceuticals LLC | 14789-137 | 14789-137-05 | 25 VIAL, GLASS in 1 CARTON (14789-137-05) / 20 mL in 1 VIAL, GLASS (14789-137-07) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2MEQ/ML | ||||
| Approval Date: | Aug 14, 2023 | TE: | AP | RLD: | No | ||||
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