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ATORVASTATIN CALCIUM - 60505-2671-0 - (ATORVASTATIN CALCIUM)

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Drug Information of ATORVASTATIN CALCIUM

Product NDC: 60505-2671
Proprietary Name: ATORVASTATIN CALCIUM
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 ATORVASTATIN CALCIUM

Product NDC: 60505-2671
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090548
Marketing Category: ANDA
Start Marketing Date: 20120529

Package Information of ATORVASTATIN CALCIUM

Package NDC: 60505-2671-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2671-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ATORVASTATIN CALCIUM

NDC Code 60505-2671-0
Proprietary Name ATORVASTATIN CALCIUM
Package Description 10 BLISTER PACK in 1 CARTON (60505-2671-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2671
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATORVASTATIN CALCIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120529
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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 ATORVASTATIN CALCIUM


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