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Atorvastatin Calcium - 0781-5381-34 - (atorvastatin calcium)

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Drug Information of Atorvastatin Calcium

Product NDC: 0781-5381
Proprietary Name: Atorvastatin Calcium
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 Atorvastatin Calcium

Product NDC: 0781-5381
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077575
Marketing Category: ANDA
Start Marketing Date: 20120529

Package Information of Atorvastatin Calcium

Package NDC: 0781-5381-34
Package Description: 3000 TABLET, FILM COATED in 1 BOTTLE (0781-5381-34)

NDC Information of Atorvastatin Calcium

NDC Code 0781-5381-34
Proprietary Name Atorvastatin Calcium
Package Description 3000 TABLET, FILM COATED in 1 BOTTLE (0781-5381-34)
Product NDC 0781-5381
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 Sandoz Inc
Substance Name ATORVASTATIN CALCIUM
Strength Number 10
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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