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"70518-0073-8" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BLISTER PACK (70518-0073-8)
(REMEDYREPACK INC.)

NDC Code70518-0073-8
Package Description21 TABLET in 1 BLISTER PACK (70518-0073-8)
Product NDC70518-0073
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20161220
Marketing Category NameANDA
Application NumberANDA085162
ManufacturerREMEDYREPACK INC.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0073-8





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