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pravastatin sodium - 68084-502-01 - (pravastatin sodium)

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Drug Information of pravastatin sodium

Product NDC: 68084-502
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: 68084-502
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077751
Marketing Category: ANDA
Start Marketing Date: 20130524

Package Information of pravastatin sodium

Package NDC: 68084-502-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-502-01) > 10 TABLET in 1 BLISTER PACK (68084-502-11)

NDC Information of pravastatin sodium

NDC Code 68084-502-01
Proprietary Name pravastatin sodium
Package Description 10 BLISTER PACK in 1 CARTON (68084-502-01) > 10 TABLET in 1 BLISTER PACK (68084-502-11)
Product NDC 68084-502
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pravastatin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130524
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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