Details for New Drug Application (NDA): 214108
✉ Email this page to a colleague
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 214108
Tradename: | POTASSIUM CHLORIDE |
Applicant: | Rubicon |
Ingredient: | potassium chloride |
Patents: | 0 |
Pharmacology for NDA: 214108
Mechanism of Action | Osmotic Activity |
Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 214108
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 214108 | ANDA | Advagen Pharma Limited | 72888-024 | 72888-024-07 | 30 POUCH in 1 CARTON (72888-024-07) / 1.58 g in 1 POUCH (72888-024-06) |
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 214108 | ANDA | Advagen Pharma Limited | 72888-024 | 72888-024-10 | 100 POUCH in 1 CARTON (72888-024-10) / 1.58 g in 1 POUCH (72888-024-06) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SOLUTION;ORAL | Strength | 20MEQ | ||||
Approval Date: | Mar 24, 2022 | TE: | AA | RLD: | No |
Complete Access Available with Subscription