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ATORVASTATIN CALCIUM - 68645-458-70 - (ATORVASTATIN CALCIUM)

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Drug Information of ATORVASTATIN CALCIUM

Product NDC: 68645-458
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: 68645-458
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020702
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130101

Package Information of ATORVASTATIN CALCIUM

Package NDC: 68645-458-70
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (68645-458-70)

NDC Information of ATORVASTATIN CALCIUM

NDC Code 68645-458-70
Proprietary Name ATORVASTATIN CALCIUM
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (68645-458-70)
Product NDC 68645-458
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATORVASTATIN CALCIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130101
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Legacy Pharmaceutical Packaging
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