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PRAVASTATIN SODIUM - 68180-487-09 - (PRAVASTATIN SODIUM)

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Drug Information of PRAVASTATIN SODIUM

Product NDC: 68180-487
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: 68180-487
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077917
Marketing Category: ANDA
Start Marketing Date: 20080724

Package Information of PRAVASTATIN SODIUM

Package NDC: 68180-487-09
Package Description: 90 TABLET in 1 BOTTLE (68180-487-09)

NDC Information of PRAVASTATIN SODIUM

NDC Code 68180-487-09
Proprietary Name PRAVASTATIN SODIUM
Package Description 90 TABLET in 1 BOTTLE (68180-487-09)
Product NDC 68180-487
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAVASTATIN SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080724
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, 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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