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Atorvastatin Calcium - 63629-4850-1 - (Atorvastatin Calcium)

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Drug Information of Atorvastatin Calcium

Product NDC: 63629-4850
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: 63629-4850
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076477
Marketing Category: ANDA
Start Marketing Date: 20111201

Package Information of Atorvastatin Calcium

Package NDC: 63629-4850-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-4850-1)

NDC Information of Atorvastatin Calcium

NDC Code 63629-4850-1
Proprietary Name Atorvastatin Calcium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-4850-1)
Product NDC 63629-4850
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atorvastatin Calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111201
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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