Lovastatin - 0615-7685-39 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 0615-7685
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: 0615-7685
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075828
Marketing Category: ANDA
Start Marketing Date: 20011217

Package Information of Lovastatin

Package NDC: 0615-7685-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7685-39)

NDC Information of Lovastatin

NDC Code 0615-7685-39
Proprietary Name Lovastatin
Package Description 30 TABLET in 1 BLISTER PACK (0615-7685-39)
Product NDC 0615-7685
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 NCS HealthCare of KY, Inc dba Vangard Labs
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