"16714-813-03" National Drug Code (NDC)

Ezetimibe 500 TABLET in 1 BOTTLE (16714-813-03)
(NorthStar Rx LLC)

NDC Code16714-813-03
Package Description500 TABLET in 1 BOTTLE (16714-813-03)
Product NDC16714-813
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20210201
Marketing Category NameANDA
Application NumberANDA209838
ManufacturerNorthStar Rx LLC
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

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