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"25208-200-15" National Drug Code (NDC)

Zypitamag 500 TABLET, FILM COATED in 1 BOTTLE (25208-200-15)
(Medicure International Inc)

NDC Code25208-200-15
Package Description500 TABLET, FILM COATED in 1 BOTTLE (25208-200-15)
Product NDC25208-200
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
Strength1
Strength Unitmg/1
Pharmacy ClassesHydroxymethylglutaryl-CoA Reductase Inhibitors [MoA],HMG-CoA Reductase Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/25208-200-15





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