"57237-165-99" National Drug Code (NDC)

NDC Code	57237-165-99
Package Description	1000 TABLET in 1 BOTTLE (57237-165-99)
Product NDC	57237-165
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pravastatin Sodium
Non-Proprietary Name	Pravastatin Sodium
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170202
Marketing Category Name	ANDA
Application Number	ANDA203367
Manufacturer	Rising Health, LLC
Substance Name	PRAVASTATIN SODIUM
Strength	20
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]