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Pravastatin Sodium - 49349-293-02 - (Pravastatin Sodium)

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Drug Information of Pravastatin Sodium

Product NDC: 49349-293
Proprietary Name: Pravastatin Sodium
Non Proprietary Name: Pravastatin Sodium
Active Ingredient(s): 20    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: 49349-293
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076714
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Pravastatin Sodium

Package NDC: 49349-293-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-293-02)

NDC Information of Pravastatin Sodium

NDC Code 49349-293-02
Proprietary Name Pravastatin Sodium
Package Description 30 TABLET in 1 BLISTER PACK (49349-293-02)
Product NDC 49349-293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PRAVASTATIN SODIUM
Strength Number 20
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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