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PRAVASTATIN SODIUM - 52125-549-02 - (PRAVASTATIN SODIUM)

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Drug Information of PRAVASTATIN SODIUM

Product NDC: 52125-549
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: 52125-549
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076341
Marketing Category: ANDA
Start Marketing Date: 20130523

Package Information of PRAVASTATIN SODIUM

Package NDC: 52125-549-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-549-02)

NDC Information of PRAVASTATIN SODIUM

NDC Code 52125-549-02
Proprietary Name PRAVASTATIN SODIUM
Package Description 30 TABLET in 1 BLISTER PACK (52125-549-02)
Product NDC 52125-549
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAVASTATIN SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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