"70518-2115-0" National Drug Code (NDC)

Prednisone 30 TABLET in 1 BLISTER PACK (70518-2115-0)
(REMEDYREPACK INC.)

NDC Code70518-2115-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2115-0)
Product NDC70518-2115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20190523
Marketing Category NameANDA
Application NumberANDA088832
ManufacturerREMEDYREPACK INC.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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