"76333-170-13" National Drug Code (NDC)

Ezetimibe 500 TABLET in 1 BOTTLE (76333-170-13)
(Orient Pharma Co., Ltd.)

NDC Code76333-170-13
Package Description500 TABLET in 1 BOTTLE (76333-170-13)
Product NDC76333-170
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20220630
Marketing Category NameANDA
Application NumberANDA215693
ManufacturerOrient Pharma Co., Ltd.
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

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