"52959-629-30" National Drug Code (NDC)

NDC Code	52959-629-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (52959-629-30)
Product NDC	52959-629
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Crestor
Non-Proprietary Name	Rosuvastatin Calcium
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20110721
Marketing Category Name	NDA
Application Number	NDA021366
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	ROSUVASTATIN CALCIUM
Strength	20
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]