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Pravastatin Sodium - 68462-198-05 - (Pravastatin Sodium)

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Drug Information of Pravastatin Sodium

Product NDC: 68462-198
Proprietary Name: Pravastatin Sodium
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 Sodium

Product NDC: 68462-198
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077987
Marketing Category: ANDA
Start Marketing Date: 20071228

Package Information of Pravastatin Sodium

Package NDC: 68462-198-05
Package Description: 500 TABLET in 1 BOTTLE (68462-198-05)

NDC Information of Pravastatin Sodium

NDC Code 68462-198-05
Proprietary Name Pravastatin Sodium
Package Description 500 TABLET in 1 BOTTLE (68462-198-05)
Product NDC 68462-198
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071228
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
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 Sodium


General Information