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amlodipine besylate and atorvastatin calcium - 54868-6335-0 - (amlodipine besylate and atorvastatin calcium)

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Drug Information of amlodipine besylate and atorvastatin calcium

Product NDC: 54868-6335
Proprietary Name: amlodipine besylate and atorvastatin calcium
Non Proprietary Name: amlodipine besylate and atorvastatin calcium
Active Ingredient(s): 10; 80    mg/1; mg/1 & nbsp;   amlodipine besylate and atorvastatin calcium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of amlodipine besylate and atorvastatin calcium

Product NDC: 54868-6335
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021540
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120308

Package Information of amlodipine besylate and atorvastatin calcium

Package NDC: 54868-6335-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-6335-0)

NDC Information of amlodipine besylate and atorvastatin calcium

NDC Code 54868-6335-0
Proprietary Name amlodipine besylate and atorvastatin calcium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-6335-0)
Product NDC 54868-6335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate and atorvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120308
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM
Strength Number 10; 80
Strength Unit mg/1; mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of amlodipine besylate and atorvastatin calcium


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