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Atorvastatin Calcium - 51079-412-03 - (atorvastatin calcium)

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Drug Information of Atorvastatin Calcium

Product NDC: 51079-412
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: 51079-412
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091226
Marketing Category: ANDA
Start Marketing Date: 20121227

Package Information of Atorvastatin Calcium

Package NDC: 51079-412-03
Package Description: 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-412-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-412-01)

NDC Information of Atorvastatin Calcium

NDC Code 51079-412-03
Proprietary Name Atorvastatin Calcium
Package Description 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-412-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-412-01)
Product NDC 51079-412
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atorvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121227
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
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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