Lovastatin - 68084-560-01 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 68084-560
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: 68084-560
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075828
Marketing Category: ANDA
Start Marketing Date: 20130709

Package Information of Lovastatin

Package NDC: 68084-560-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-560-01) > 10 TABLET in 1 BLISTER PACK (68084-560-11)

NDC Information of Lovastatin

NDC Code 68084-560-01
Proprietary Name Lovastatin
Package Description 10 BLISTER PACK in 1 CARTON (68084-560-01) > 10 TABLET in 1 BLISTER PACK (68084-560-11)
Product NDC 68084-560
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130709
Marketing Category Name ANDA
Labeler Name American Health Packaging
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