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ATORVASTATIN CALCIUM - 55154-2096-0 - (ATORVASTATIN CALCIUM)

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Drug Information of ATORVASTATIN CALCIUM

Product NDC: 55154-2096
Proprietary Name: ATORVASTATIN CALCIUM
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 ATORVASTATIN CALCIUM

Product NDC: 55154-2096
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120116

Package Information of ATORVASTATIN CALCIUM

Package NDC: 55154-2096-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2096-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ATORVASTATIN CALCIUM

NDC Code 55154-2096-0
Proprietary Name ATORVASTATIN CALCIUM
Package Description 10 BLISTER PACK in 1 BAG (55154-2096-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-2096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATORVASTATIN CALCIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120116
Marketing Category Name NDA AUTHORIZED GENERIC
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 ATORVASTATIN CALCIUM


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