"61919-995-07" National Drug Code (NDC)

Prednisone 7 TABLET in 1 BOTTLE (61919-995-07)
(DirectRX)

NDC Code61919-995-07
Package Description7 TABLET in 1 BOTTLE (61919-995-07)
Product NDC61919-995
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA084283
ManufacturerDirectRX
Substance NamePREDNISONE
Strength50
Strength Unitmg/1
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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