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"52125-730-02" National Drug Code (NDC)

Zetia 30 TABLET in 1 BOTTLE (52125-730-02)
(REMEDYREPACK INC.)

NDC Code52125-730-02
Package Description30 TABLET in 1 BOTTLE (52125-730-02)
Product NDC52125-730
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZetia
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20131004
Marketing Category NameNDA
Application NumberNDA021445
ManufacturerREMEDYREPACK INC.
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-730-02





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