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PRAVASTATIN SODIUM - 0904-5892-61 - (PRAVASTATIN SODIUM)

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Drug Information of PRAVASTATIN SODIUM

Product NDC: 0904-5892
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: 0904-5892
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076341
Marketing Category: ANDA
Start Marketing Date: 20080801

Package Information of PRAVASTATIN SODIUM

Package NDC: 0904-5892-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5892-61)

NDC Information of PRAVASTATIN SODIUM

NDC Code 0904-5892-61
Proprietary Name PRAVASTATIN SODIUM
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5892-61)
Product NDC 0904-5892
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAVASTATIN SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080801
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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