"60219-1069-5" National Drug Code (NDC)

Potassium Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-1069-5)
(Amneal Pharmaceuticals NY LLC)

NDC Code60219-1069-5
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-1069-5)
Product NDC60219-1069
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 ClassesPotassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]

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