Lovastatin - 55289-881-30 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 55289-881
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: 55289-881
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078296
Marketing Category: ANDA
Start Marketing Date: 20071101

Package Information of Lovastatin

Package NDC: 55289-881-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-881-30)

NDC Information of Lovastatin

NDC Code 55289-881-30
Proprietary Name Lovastatin
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-881-30)
Product NDC 55289-881
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071101
Marketing Category Name ANDA
Labeler Name PD-Rx 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