Lovastatin - 0093-0576-93 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 0093-0576
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: 0093-0576
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075551
Marketing Category: ANDA
Start Marketing Date: 20011217

Package Information of Lovastatin

Package NDC: 0093-0576-93
Package Description: 100 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (0093-0576-93) > 1 TABLET in 1 BLISTER PACK (0093-0576-19)

NDC Information of Lovastatin

NDC Code 0093-0576-93
Proprietary Name Lovastatin
Package Description 100 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (0093-0576-93) > 1 TABLET in 1 BLISTER PACK (0093-0576-19)
Product NDC 0093-0576
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20011217
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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