"70882-117-21" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BLISTER PACK (70882-117-21)
(Cambridge Therapeutics Technologies, LLC)

NDC Code70882-117-21
Package Description21 TABLET in 1 BLISTER PACK (70882-117-21)
Product NDC70882-117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20010829
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerCambridge Therapeutics Technologies, LLC
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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