"52125-957-03" National Drug Code (NDC)

Prednisone 20 TABLET in 1 BOTTLE (52125-957-03)
(REMEDYREPACK INC.)

NDC Code52125-957-03
Package Description20 TABLET in 1 BOTTLE (52125-957-03)
Product NDC52125-957
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20140904
End Marketing Date20170425
Marketing Category NameANDA
Application NumberANDA088832
ManufacturerREMEDYREPACK INC.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1

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