Lipitor - 63629-3366-4 - (ATORVASTATIN CALCIUM)

Alphabetical Index


Drug Information of Lipitor

Product NDC: 63629-3366
Proprietary Name: Lipitor
Non Proprietary Name: ATORVASTATIN CALCIUM
Active Ingredient(s): 80    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: 63629-3366
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA
Start Marketing Date: 20000407

Package Information of Lipitor

Package NDC: 63629-3366-4
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE (63629-3366-4)

NDC Information of Lipitor

NDC Code 63629-3366-4
Proprietary Name Lipitor
Package Description 180 TABLET, FILM COATED in 1 BOTTLE (63629-3366-4)
Product NDC 63629-3366
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATORVASTATIN CALCIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000407
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name ATORVASTATIN CALCIUM
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lipitor


General Information