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"68001-567-03" National Drug Code (NDC)

Potassium Chloride Extended-release 500 TABLET in 1 BOTTLE (68001-567-03)
(Bluepoint Laboratories)

NDC Code68001-567-03
Package Description500 TABLET in 1 BOTTLE (68001-567-03)
Product NDC68001-567
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride Extended-release
Non-Proprietary NamePotassium Chloride Extended-release
Dosage FormTABLET
UsageORAL
Start Marketing Date20210130
Marketing Category NameANDA
Application NumberANDA214452
ManufacturerBluepoint Laboratories
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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