"70518-2262-0" National Drug Code (NDC)

Ezetimibe 90 TABLET in 1 BOTTLE, PLASTIC (70518-2262-0)
(REMEDYREPACK INC.)

NDC Code70518-2262-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-2262-0)
Product NDC70518-2262
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20190812
Marketing Category NameANDA
Application NumberANDA209234
ManufacturerREMEDYREPACK INC.
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

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