Details for New Drug Application (NDA): 019123
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The generic ingredient in KLOR-CON is potassium chloride. There are two hundred and forty drug master file entries for this compound. Eighty-one suppliers are listed for this compound. Additional details are available on the potassium chloride profile page.
Summary for 019123
| Tradename: | KLOR-CON |
| Applicant: | Upsher Smith Labs |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 019123
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 019123
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| KLOR-CON | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 019123 | NDA | Upsher-Smith Laboratories, LLC | 0245-5315 | 0245-5315-01 | 100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89) |
| KLOR-CON | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 019123 | NDA | Upsher-Smith Laboratories, LLC | 0245-5315 | 0245-5315-11 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-11) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 8MEQ | ||||
| Approval Date: | Apr 17, 1986 | TE: | AB2 | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 10MEQ | ||||
| Approval Date: | Apr 17, 1986 | TE: | AB2 | RLD: | Yes | ||||
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