"43063-443-90" National Drug Code (NDC)

NDC Code	43063-443-90
Package Description	90 TABLET in 1 BOTTLE, PLASTIC (43063-443-90)
Product NDC	43063-443
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pravastatin Sodium
Non-Proprietary Name	Pravastatin Sodium
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20100330
Marketing Category Name	ANDA
Application Number	ANDA077751
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	PRAVASTATIN SODIUM
Strength	20
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]