"61919-108-20" National Drug Code (NDC)

Prednisone 20 TABLET in 1 BOTTLE (61919-108-20)
(Direct_Rx)

NDC Code61919-108-20
Package Description20 TABLET in 1 BOTTLE (61919-108-20)
Product NDC61919-108
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20190807
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerDirect_Rx
Substance NamePREDNISONE
Strength20
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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