Lovastatin - 68788-2634-9 - (Lovastatin)

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Drug Information of Lovastatin

Product NDC: 68788-2634
Proprietary Name: Lovastatin
Non Proprietary Name: Lovastatin
Active Ingredient(s): 20    mg/1 & nbsp;   Lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lovastatin

Product NDC: 68788-2634
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075828
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of Lovastatin

Package NDC: 68788-2634-9
Package Description: 90 TABLET in 1 BOTTLE (68788-2634-9)

NDC Information of Lovastatin

NDC Code 68788-2634-9
Proprietary Name Lovastatin
Package Description 90 TABLET in 1 BOTTLE (68788-2634-9)
Product NDC 68788-2634
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name LOVASTATIN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lovastatin


General Information