"70518-3476-0" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BLISTER PACK (70518-3476-0)
(REMEDYREPACK INC.)

NDC Code70518-3476-0
Package Description21 TABLET in 1 BLISTER PACK (70518-3476-0)
Product NDC70518-3476
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20220816
Marketing Category NameANDA
Application NumberANDA208412
ManufacturerREMEDYREPACK INC.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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