Lipitor - 49999-467-90 - (atorvastatin calcium)

Alphabetical Index


Drug Information of Lipitor

Product NDC: 49999-467
Proprietary Name: Lipitor
Non Proprietary Name: atorvastatin calcium
Active Ingredient(s): 20    mg/1 & nbsp;   atorvastatin calcium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lipitor

Product NDC: 49999-467
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA
Start Marketing Date: 20120305

Package Information of Lipitor

Package NDC: 49999-467-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (49999-467-90)

NDC Information of Lipitor

NDC Code 49999-467-90
Proprietary Name Lipitor
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (49999-467-90)
Product NDC 49999-467
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atorvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ATORVASTATIN CALCIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lipitor


General Information