"60687-736-09" National Drug Code (NDC)

Pantoprazole Sodium 80 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
(American Health Packaging)

NDC Code60687-736-09
Package Description80 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
Product NDC60687-736
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePantoprazole Sodium
Non-Proprietary NamePantoprazole Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20230705
Marketing Category NameANDA
Application NumberANDA202038
ManufacturerAmerican Health Packaging
Substance NamePANTOPRAZOLE SODIUM
Strength40
Strength Unitmg/1
Pharmacy ClassesProton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

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