FDA.reportPublic FDA data

Application 077793

Type
ANDA
Sponsor
TEVA PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001PRAVASTATIN SODIUMPRAVASTATIN SODIUMTABLET;ORAL80MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7270Pravastatin SodiumPravastatin SodiumTeva Pharmaceuticals USA, Inc.ANDACurrent
0615-7740Pravastatin SodiumPravastatin SodiumNCS HealthCare of KY, Inc dba Vangard LabsANDACurrent
0615-8159Pravastatin SodiumPravastatin SodiumNCS HealthCare of KY, Inc dba Vangard LabsANDACurrent
0615-8159Pravastatin SodiumPravastatin SodiumNCS HealthCare of KY, LLC dba Vangard LabsANDACurrent
42291-669Pravastatin SodiumPravastatin SodiumAvKARE, Inc.ANDACurrent
42291-669Pravastatin SodiumPravastatin SodiumAvKAREANDACurrent
42291-669Pravastatin SodiumPravastatin SodiumAvKAREANDACurrent
42291-669Pravastatin SodiumPravastatin SodiumAvKAREANDACurrent
43353-966Pravastatin SodiumPravastatin SodiumAphena Pharma Solutions - Tennessee, LLCANDACurrent
43353-966Pravastatin SodiumPravastatin SodiumAphena Pharma Solutions - Tennessee, LLCANDACurrent
50090-5927Pravastatin SodiumPravastatin SodiumA-S Medication SolutionsANDACurrent
70518-2986Pravastatin SodiumPravastatin SodiumREMEDYREPACK INC.ANDACurrent