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ATORVASTATIN CALCIUM - 0904-6291-61 - (ATORVASTATIN CALCIUM)

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Drug Information of ATORVASTATIN CALCIUM

Product NDC: 0904-6291
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: 0904-6291
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090548
Marketing Category: ANDA
Start Marketing Date: 20120529

Package Information of ATORVASTATIN CALCIUM

Package NDC: 0904-6291-61
Package Description: 100 TABLET, FILM COATED in 1 BLISTER PACK (0904-6291-61)

NDC Information of ATORVASTATIN CALCIUM

NDC Code 0904-6291-61
Proprietary Name ATORVASTATIN CALCIUM
Package Description 100 TABLET, FILM COATED in 1 BLISTER PACK (0904-6291-61)
Product NDC 0904-6291
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 Major Pharmaceuticals
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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