Details for New Drug Application (NDA): 205993
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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 205993
Tradename: | POTASSIUM CHLORIDE |
Applicant: | Padagis Us |
Ingredient: | potassium chloride |
Patents: | 0 |
Pharmacology for NDA: 205993
Mechanism of Action | Osmotic Activity |
Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 205993
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM CHLORIDE | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 205993 | ANDA | Padagis US LLC | 0574-0275 | 0574-0275-11 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
POTASSIUM CHLORIDE | potassium chloride | TABLET, EXTENDED RELEASE;ORAL | 205993 | ANDA | Cardinal Health 107, LLC | 55154-6709 | 55154-6709-0 | 10 BLISTER PACK in 1 BAG (55154-6709-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 8MEQ | ||||
Approval Date: | Nov 5, 2015 | TE: | AB2 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 10MEQ | ||||
Approval Date: | Nov 5, 2015 | TE: | AB2 | RLD: | No |
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