Details for New Drug Application (NDA): 210733
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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 210733
| Tradename: | POTASSIUM CHLORIDE |
| Applicant: | Strides Pharma |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 210733
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 210733
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 210733 | ANDA | Northwind Pharmaceuticals | 51655-706 | 51655-706-52 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-706-52) |
| POTASSIUM CHLORIDE | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 210733 | ANDA | Strides Pharma Science Limited | 64380-860 | 64380-860-06 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 8MEQ | ||||
| Approval Date: | Aug 31, 2018 | TE: | AB2 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 10MEQ | ||||
| Approval Date: | Aug 31, 2018 | TE: | AB2 | RLD: | No | ||||
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