"70934-880-21" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE, PLASTIC (70934-880-21)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-880-21
Package Description21 TABLET in 1 BOTTLE, PLASTIC (70934-880-21)
Product NDC70934-880
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20210802
End Marketing Date20240531
Marketing Category NameANDA
Application NumberANDA080292
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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