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Pravastatin sodium - 43063-195-30 - (Pravastatin sodium)

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Drug Information of Pravastatin sodium

Product NDC: 43063-195
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: 43063-195
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076714
Marketing Category: ANDA
Start Marketing Date: 20091231

Package Information of Pravastatin sodium

Package NDC: 43063-195-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-195-30)

NDC Information of Pravastatin sodium

NDC Code 43063-195-30
Proprietary Name Pravastatin sodium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-195-30)
Product NDC 43063-195
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091231
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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