Caduet - 0069-2170-30 - (amlodipine besylate and atorvastatin calcium)

Alphabetical Index


Drug Information of Caduet

Product NDC: 0069-2170
Proprietary Name: Caduet
Non Proprietary Name: amlodipine besylate and atorvastatin calcium
Active Ingredient(s): 5; 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: 0069-2170
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021540
Marketing Category: NDA
Start Marketing Date: 20040130

Package Information of Caduet

Package NDC: 0069-2170-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0069-2170-30)

NDC Information of Caduet

NDC Code 0069-2170-30
Proprietary Name Caduet
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0069-2170-30)
Product NDC 0069-2170
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 20040130
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM
Strength Number 5; 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