"0603-1567-56" National Drug Code (NDC)

Prednisolone 240 mL in 1 BOTTLE (0603-1567-56)
(Par Pharmaceutical)

NDC Code0603-1567-56
Package Description240 mL in 1 BOTTLE (0603-1567-56)
Product NDC0603-1567
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisolone
Non-Proprietary NamePrednisolone
Dosage FormSYRUP
UsageORAL
Start Marketing Date20070921
End Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA040775
ManufacturerPar Pharmaceutical
Substance NamePREDNISOLONE
Strength15
Strength Unitmg/5mL
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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