Lovastatin - 49349-531-02 - (Lovastatin)

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Drug Information of Lovastatin

Product NDC: 49349-531
Proprietary Name: Lovastatin
Non Proprietary Name: Lovastatin
Active Ingredient(s): 40    mg/1 & nbsp;   Lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lovastatin

Product NDC: 49349-531
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075828
Marketing Category: ANDA
Start Marketing Date: 20110923

Package Information of Lovastatin

Package NDC: 49349-531-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-531-02)

NDC Information of Lovastatin

NDC Code 49349-531-02
Proprietary Name Lovastatin
Package Description 30 TABLET in 1 BLISTER PACK (49349-531-02)
Product NDC 49349-531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110923
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LOVASTATIN
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lovastatin


General Information