"60687-708-09" National Drug Code (NDC)

Potassium Chloride 80 BLISTER PACK in 1 CARTON (60687-708-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-708-11)
(American Health Packaging)

NDC Code60687-708-09
Package Description80 BLISTER PACK in 1 CARTON (60687-708-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-708-11)
Product NDC60687-708
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230227
End Marketing Date20241031
Marketing Category NameANDA
Application NumberANDA210733
ManufacturerAmerican Health Packaging
Substance NamePOTASSIUM CHLORIDE
Strength750
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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