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Pravastatin Sodium - 55154-5370-0 - (Pravastatin Sodium)

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Drug Information of Pravastatin Sodium

Product NDC: 55154-5370
Proprietary Name: Pravastatin Sodium
Non Proprietary Name: Pravastatin Sodium
Active Ingredient(s): 40    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: 55154-5370
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076056
Marketing Category: ANDA
Start Marketing Date: 20120210

Package Information of Pravastatin Sodium

Package NDC: 55154-5370-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-5370-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Pravastatin Sodium

NDC Code 55154-5370-0
Proprietary Name Pravastatin Sodium
Package Description 1 BLISTER PACK in 1 BAG (55154-5370-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 55154-5370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120210
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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