"25208-200-09" National Drug Code (NDC)

NDC Code	25208-200-09
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (25208-200-09)
Product NDC	25208-200
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zypitamag
Non-Proprietary Name	Pitavastatin Magnesium
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180309
End Marketing Date	20210531
Marketing Category Name	NDA
Application Number	NDA208379
Manufacturer	Medicure International Inc
Substance Name	PITAVASTATIN
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA],HMG-CoA Reductase Inhibitor [EPC]