Details for New Drug Application (NDA): 210200
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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 210200
Tradename: | POTASSIUM CHLORIDE |
Applicant: | Epic Pharma Llc |
Ingredient: | potassium chloride |
Patents: | 0 |
Pharmacology for NDA: 210200
Mechanism of Action | Osmotic Activity |
Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 210200
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210200 | ANDA | Epic Pharma, LLC | 42806-094 | 42806-094-01 | 100 PACKET in 1 CARTON (42806-094-01) / 1.77 g in 1 PACKET (42806-094-99) |
POTASSIUM CHLORIDE | potassium chloride | FOR SOLUTION;ORAL | 210200 | ANDA | Epic Pharma, LLC | 42806-094 | 42806-094-30 | 30 PACKET in 1 CARTON (42806-094-30) / 1.77 g in 1 PACKET (42806-094-99) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SOLUTION;ORAL | Strength | 20MEQ | ||||
Approval Date: | Nov 23, 2018 | TE: | AA | RLD: | No |
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