"50228-379-90" National Drug Code (NDC)

Ezetimibe 90 TABLET in 1 BOTTLE (50228-379-90)
(ScieGen Pharmaceuticals Inc)

NDC Code50228-379-90
Package Description90 TABLET in 1 BOTTLE (50228-379-90)
Product NDC50228-379
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20201023
Marketing Category NameANDA
Application NumberANDA210673
ManufacturerScieGen Pharmaceuticals Inc
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

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