"42708-115-21" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (42708-115-21)
(QPharma Inc)

NDC Code42708-115-21
Package Description21 TABLET in 1 BOTTLE (42708-115-21)
Product NDC42708-115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date19900101
Marketing Category NameANDA
Application NumberANDA085162
ManufacturerQPharma Inc
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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