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PRAVASTATIN SODIUM - 60505-0170-7 - (PRAVASTATIN SODIUM)

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Drug Information of PRAVASTATIN SODIUM

Product NDC: 60505-0170
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: 60505-0170
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076341
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of PRAVASTATIN SODIUM

Package NDC: 60505-0170-7
Package Description: 1000 TABLET in 1 BOTTLE (60505-0170-7)

NDC Information of PRAVASTATIN SODIUM

NDC Code 60505-0170-7
Proprietary Name PRAVASTATIN SODIUM
Package Description 1000 TABLET in 1 BOTTLE (60505-0170-7)
Product NDC 60505-0170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAVASTATIN SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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