"53002-3520-1" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (53002-3520-1)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-3520-1
Package Description21 TABLET in 1 BOTTLE (53002-3520-1)
Product NDC53002-3520
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date19900101
Marketing Category NameANDA
Application NumberANDA080356
ManufacturerRPK Pharmaceuticals, Inc.
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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