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Atorvastatin Calcium - 55111-121-90 - (Atorvastatin Calcium)

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Drug Information of Atorvastatin Calcium

Product NDC: 55111-121
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
Coding System: National Drug Codes(NDC)

Labeler Information of Atorvastatin Calcium

Product NDC: 55111-121
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091650
Marketing Category: ANDA
Start Marketing Date: 20120717

Package Information of Atorvastatin Calcium

Package NDC: 55111-121-90
Package Description: 90 TABLET in 1 BOTTLE (55111-121-90)

NDC Information of Atorvastatin Calcium

NDC Code 55111-121-90
Proprietary Name Atorvastatin Calcium
Package Description 90 TABLET in 1 BOTTLE (55111-121-90)
Product NDC 55111-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atorvastatin Calcium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120717
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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


General Information