"53002-3090-3" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (53002-3090-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-3090-3
Package Description21 TABLET in 1 BOTTLE (53002-3090-3)
Product NDC53002-3090
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20010829
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerRPK Pharmaceuticals, Inc.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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