Details for New Drug Application (NDA): 210241
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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 210241
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Novel Labs Inc |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 210241
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 210241
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210241 | ANDA | Novel Laboratories, Inc. | 40032-194 | 40032-194-30 | 30 POUCH in 1 CARTON (40032-194-30) / 1.5 g in 1 POUCH (40032-194-90) |
| POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210241 | ANDA | Novel Laboratories, Inc. | 40032-194 | 40032-194-31 | 100 POUCH in 1 CARTON (40032-194-31) / 1.5 g in 1 POUCH (40032-194-90) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SOLUTION;ORAL | Strength | 20MEQ | ||||
| Approval Date: | Nov 21, 2018 | TE: | AA | RLD: | No | ||||
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