"50436-1720-5" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (50436-1720-5)
(Unit Dose Services)

NDC Code50436-1720-5
Package Description21 TABLET in 1 BOTTLE (50436-1720-5)
Product NDC50436-1720
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20010829
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerUnit Dose Services
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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