Caduet - 54868-5209-0 - (amlodipine besylate and atorvastatin calcium)

Alphabetical Index


Drug Information of Caduet

Product NDC: 54868-5209
Proprietary Name: Caduet
Non Proprietary Name: amlodipine besylate and atorvastatin calcium
Active Ingredient(s): 10; 20    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 Caduet

Product NDC: 54868-5209
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021540
Marketing Category: NDA
Start Marketing Date: 20050118

Package Information of Caduet

Package NDC: 54868-5209-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5209-0)

NDC Information of Caduet

NDC Code 54868-5209-0
Proprietary Name Caduet
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5209-0)
Product NDC 54868-5209
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 20050118
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM
Strength Number 10; 20
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 Caduet


General Information