Details for New Drug Application (NDA): 210902
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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 210902
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Amneal |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 210902
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 210902
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210902 | ANDA | Amneal Pharmaceuticals LLC | 60219-1617 | 60219-1617-3 | 30 POUCH in 1 CARTON (60219-1617-3) / 1.58 g in 1 POUCH (60219-1617-1) |
| POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210902 | ANDA | Amneal Pharmaceuticals LLC | 60219-1617 | 60219-1617-8 | 100 POUCH in 1 CARTON (60219-1617-8) / 1.58 g in 1 POUCH (60219-1617-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SOLUTION;ORAL | Strength | 20MEQ | ||||
| Approval Date: | May 23, 2019 | TE: | AA | RLD: | No | ||||
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