Details for New Drug Application (NDA): 214076
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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 214076
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Tris Pharma Inc |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 214076
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 214076
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | SOLUTION;ORAL | 214076 | ANDA | Tris Pharma Inc | 27808-168 | 27808-168-01 | 473 mL in 1 BOTTLE (27808-168-01) |
| POTASSIUM CHLORIDE | potassium chloride | SOLUTION;ORAL | 214076 | ANDA | Tris Pharma Inc | 27808-169 | 27808-169-01 | 473 mL in 1 BOTTLE (27808-169-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;ORAL | Strength | 20MEQ/15ML | ||||
| Approval Date: | Jan 26, 2022 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;ORAL | Strength | 40MEQ/15ML | ||||
| Approval Date: | Jan 26, 2022 | TE: | RLD: | No | |||||
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