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Pravastatin Sodium - 0093-7201-98 - (Pravastatin Sodium)

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Drug Information of Pravastatin Sodium

Product NDC: 0093-7201
Proprietary Name: Pravastatin Sodium
Non Proprietary Name: Pravastatin Sodium
Active Ingredient(s): 20    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: 0093-7201
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076056
Marketing Category: ANDA
Start Marketing Date: 20060425

Package Information of Pravastatin Sodium

Package NDC: 0093-7201-98
Package Description: 90 TABLET in 1 BOTTLE (0093-7201-98)

NDC Information of Pravastatin Sodium

NDC Code 0093-7201-98
Proprietary Name Pravastatin Sodium
Package Description 90 TABLET in 1 BOTTLE (0093-7201-98)
Product NDC 0093-7201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060425
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PRAVASTATIN SODIUM
Strength Number 20
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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