"61919-235-30" National Drug Code (NDC)

Prednisone 30 TABLET in 1 BOTTLE (61919-235-30)
(DIRECT RX)

NDC Code61919-235-30
Package Description30 TABLET in 1 BOTTLE (61919-235-30)
Product NDC61919-235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerDIRECT RX
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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