"25208-202-15" National Drug Code (NDC)

Zypitamag 500 TABLET, FILM COATED in 1 BOTTLE (25208-202-15)
(Medicure International Inc)

NDC Code25208-202-15
Package Description500 TABLET, FILM COATED in 1 BOTTLE (25208-202-15)
Product NDC25208-202
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZypitamag
Non-Proprietary NamePitavastatin Magnesium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180309
Marketing Category NameNDA
Application NumberNDA208379
ManufacturerMedicure International Inc
Substance NamePITAVASTATIN
Strength4
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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