Lipitor - 49349-103-02 - (ATORVASTATIN CALCIUM)

Alphabetical Index


Drug Information of Lipitor

Product NDC: 49349-103
Proprietary Name: Lipitor
Non Proprietary Name: ATORVASTATIN CALCIUM
Active Ingredient(s): 10    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: 49349-103
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA
Start Marketing Date: 20130604

Package Information of Lipitor

Package NDC: 49349-103-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-103-02)

NDC Information of Lipitor

NDC Code 49349-103-02
Proprietary Name Lipitor
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-103-02)
Product NDC 49349-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATORVASTATIN CALCIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130604
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name ATORVASTATIN
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lipitor


General Information