"25208-200-10" National Drug Code (NDC)

Zypitamag 1 BLISTER PACK in 1 CARTON (25208-200-10) > 7 TABLET, FILM COATED in 1 BLISTER PACK
(Medicure International Inc)

NDC Code25208-200-10
Package Description1 BLISTER PACK in 1 CARTON (25208-200-10) > 7 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC25208-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZypitamag
Non-Proprietary NamePitavastatin Magnesium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180309
End Marketing Date20210531
Marketing Category NameNDA
Application NumberNDA208379
ManufacturerMedicure International Inc
Substance NamePITAVASTATIN
Strength1
Strength Unitmg/1
Pharmacy ClassesHydroxymethylglutaryl-CoA Reductase Inhibitors [MoA],HMG-CoA Reductase Inhibitor [EPC]

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