Details for New Drug Application (NDA): 212816
✉ 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 212816
Tradename: | POTASSIUM CHLORIDE |
Applicant: | Novitium Pharma |
Ingredient: | potassium chloride |
Patents: | 0 |
Pharmacology for NDA: 212816
Mechanism of Action | Osmotic Activity |
Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 212816
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 212816 | ANDA | ANI Pharmaceuticals, Inc. | 70954-197 | 70954-197-20 | 30 POUCH in 1 CARTON (70954-197-20) / 1.56 g in 1 POUCH (70954-197-10) |
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 212816 | ANDA | ANI Pharmaceuticals, Inc. | 70954-197 | 70954-197-30 | 100 POUCH in 1 CARTON (70954-197-30) / 1.56 g in 1 POUCH (70954-197-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SOLUTION;ORAL | Strength | 20MEQ | ||||
Approval Date: | Jul 12, 2023 | TE: | AA | RLD: | No |
Complete Access Available with Subscription