"16252-528-50" National Drug Code (NDC)

NDC Code	16252-528-50
Package Description	500 TABLET in 1 BOTTLE (16252-528-50)
Product NDC	16252-528
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pravastatin Sodium
Non-Proprietary Name	Pravastatin Sodium
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20061023
End Marketing Date	20190331
Marketing Category Name	ANDA
Application Number	ANDA076939
Manufacturer	Actavis Pharma, Inc.
Substance Name	PRAVASTATIN SODIUM
Strength	40
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]