"72189-275-21" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (72189-275-21)
(DIRECT RX)

NDC Code72189-275-21
Package Description21 TABLET in 1 BOTTLE (72189-275-21)
Product NDC72189-275
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20210917
Marketing Category NameANDA
Application NumberANDA211495
ManufacturerDIRECT RX
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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