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Pravastatin - 0615-7570-39 - (Pravastatin Sodium)

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Drug Information of Pravastatin

Product NDC: 0615-7570
Proprietary Name: Pravastatin
Non Proprietary Name: Pravastatin Sodium
Active Ingredient(s): 80    mg/1 & nbsp;   Pravastatin Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pravastatin

Product NDC: 0615-7570
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076714
Marketing Category: ANDA
Start Marketing Date: 20061023

Package Information of Pravastatin

Package NDC: 0615-7570-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7570-39)

NDC Information of Pravastatin

NDC Code 0615-7570-39
Proprietary Name Pravastatin
Package Description 30 TABLET in 1 BLISTER PACK (0615-7570-39)
Product NDC 0615-7570
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061023
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PRAVASTATIN SODIUM
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Pravastatin


General Information