Lipitor - 55154-2422-0 - (atorvastatin calcium)

Alphabetical Index


Drug Information of Lipitor

Product NDC: 55154-2422
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: 55154-2422
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA
Start Marketing Date: 19961217

Package Information of Lipitor

Package NDC: 55154-2422-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2422-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Lipitor

NDC Code 55154-2422-0
Proprietary Name Lipitor
Package Description 10 BLISTER PACK in 1 BAG (55154-2422-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-2422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atorvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961217
Marketing Category Name NDA
Labeler Name Cardinal Health
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