"72189-673-21" National Drug Code (NDC)

Prednisone D/p 21 TABLET in 1 BLISTER PACK (72189-673-21)
(Direct_Rx)

NDC Code72189-673-21
Package Description21 TABLET in 1 BLISTER PACK (72189-673-21)
Product NDC72189-673
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone D/p
Non-Proprietary NamePrednisone D/p
Dosage FormTABLET
UsageORAL
Start Marketing Date20260409
Marketing Category NameANDA
Application NumberANDA211575
ManufacturerDirect_Rx
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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