Lipitor - 55289-861-30 - (atorvastatin calcium trihydrate)

Alphabetical Index


Drug Information of Lipitor

Product NDC: 55289-861
Proprietary Name: Lipitor
Non Proprietary Name: atorvastatin calcium trihydrate
Active Ingredient(s): 40    mg/1 & nbsp;   atorvastatin calcium trihydrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lipitor

Product NDC: 55289-861
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA
Start Marketing Date: 19961217

Package Information of Lipitor

Package NDC: 55289-861-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-861-30)

NDC Information of Lipitor

NDC Code 55289-861-30
Proprietary Name Lipitor
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-861-30)
Product NDC 55289-861
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atorvastatin calcium trihydrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961217
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ATORVASTATIN CALCIUM TRIHYDRATE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lipitor


General Information