Lovastatin - 42254-028-90 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 42254-028
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: 42254-028
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075991
Marketing Category: ANDA
Start Marketing Date: 20021125

Package Information of Lovastatin

Package NDC: 42254-028-90
Package Description: 90 TABLET in 1 BOTTLE (42254-028-90)

NDC Information of Lovastatin

NDC Code 42254-028-90
Proprietary Name Lovastatin
Package Description 90 TABLET in 1 BOTTLE (42254-028-90)
Product NDC 42254-028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021125
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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