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ATORVASTATIN CALCIUM - 50436-9987-1 - (ATORVASTATIN CALCIUM)

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Drug Information of ATORVASTATIN CALCIUM

Product NDC: 50436-9987
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: 50436-9987
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090548
Marketing Category: ANDA
Start Marketing Date: 20120529

Package Information of ATORVASTATIN CALCIUM

Package NDC: 50436-9987-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (50436-9987-1)

NDC Information of ATORVASTATIN CALCIUM

NDC Code 50436-9987-1
Proprietary Name ATORVASTATIN CALCIUM
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (50436-9987-1)
Product NDC 50436-9987
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 Unit Dose Services
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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