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Pravastatin Sodium - 0615-6557-39 - (Pravastain Sodium)

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Drug Information of Pravastatin Sodium

Product NDC: 0615-6557
Proprietary Name: Pravastatin Sodium
Non Proprietary Name: Pravastain Sodium
Active Ingredient(s): 40    mg/1 & nbsp;   Pravastain Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pravastatin Sodium

Product NDC: 0615-6557
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076056
Marketing Category: ANDA
Start Marketing Date: 20110722

Package Information of Pravastatin Sodium

Package NDC: 0615-6557-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-6557-39)

NDC Information of Pravastatin Sodium

NDC Code 0615-6557-39
Proprietary Name Pravastatin Sodium
Package Description 30 TABLET in 1 BLISTER PACK (0615-6557-39)
Product NDC 0615-6557
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastain Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110722
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PRAVASTATIN SODIUM
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Pravastatin Sodium


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