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pravastatin sodium - 43063-444-90 - (pravastatin sodium)

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Drug Information of pravastatin sodium

Product NDC: 43063-444
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: 43063-444
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077751
Marketing Category: ANDA
Start Marketing Date: 20100330

Package Information of pravastatin sodium

Package NDC: 43063-444-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-444-90)

NDC Information of pravastatin sodium

NDC Code 43063-444-90
Proprietary Name pravastatin sodium
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-444-90)
Product NDC 43063-444
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pravastatin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100330
Marketing Category Name ANDA
Labeler Name PD-Rx 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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