"0781-5022-01" National Drug Code (NDC)

Methylprednisolone 100 TABLET in 1 BOTTLE (0781-5022-01)
(Sandoz Inc)

NDC Code0781-5022-01
Package Description100 TABLET in 1 BOTTLE (0781-5022-01)
Product NDC0781-5022
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethylprednisolone
Non-Proprietary NameMethylprednisolone
Dosage FormTABLET
UsageORAL
Start Marketing Date19971031
End Marketing Date20240131
Marketing Category NameANDA
Application NumberANDA040194
ManufacturerSandoz Inc
Substance NameMETHYLPREDNISOLONE
Strength4
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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