Potassium Chloride 60687-0810-09

Package NDC

60687-0810-09

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 20, 2024
Listing Expires: December 31, 2026
Application: ANDA210921

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Active Ingredients

Ingredient	Strength
Potassium Chloride	750 mg/1

Drug Class

Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]

Selected Package

60687-0810-09Selected

80 BLISTER PACK in 1 CARTON (60687-810-09) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-810-11)