Details for New Drug Application (NDA): 206814
The generic ingredient in POTASSIUM CHLORIDE is calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate. There are five 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 206814
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Genus Lifesciences |
| Ingredient: | potassium chloride |
| Patents: | 2 |
Pharmacology for NDA: 206814
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 206814
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POKONZA | potassium chloride | SOLUTION;ORAL | 206814 | NDA | Carwin Pharmaceutical Associates, LLC | 15370-307 | 15370-307-04 | 118 mL in 1 BOTTLE (15370-307-04) |
| POTASSIUM CHLORIDE | potassium chloride | SOLUTION;ORAL | 206814 | NDA | Carwin Pharmaceutical Associates, LLC | 15370-307 | 15370-307-04 | 118 mL in 1 BOTTLE (15370-307-04) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 20MEQ/15ML | ||||
| Approval Date: | Dec 22, 2014 | TE: | AA | RLD: | Yes | ||||
| Patent: | 12,539,314 | Patent Expiration: | Mar 7, 2039 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
| Patent: | 12,728,138 | Patent Expiration: | Mar 7, 2039 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 40MEQ/15ML | ||||
| Approval Date: | Dec 22, 2014 | TE: | AA | RLD: | Yes | ||||
| Patent: | 12,539,314 | Patent Expiration: | Mar 7, 2039 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
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