"69238-1069-5" National Drug Code (NDC)

Potassium Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1069-5)
(Amneal Pharmaceuticals NY LLC)

NDC Code69238-1069-5
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1069-5)
Product NDC69238-1069
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200511
Marketing Category NameANDA
Application NumberANDA212861
ManufacturerAmneal Pharmaceuticals NY LLC
Substance NamePOTASSIUM CHLORIDE
Strength1500
Strength Unitmg/1
Pharmacy ClassesIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]

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