Caduet (Pfizer Laboratories Div Pfizer Inc)


Welcome to the PulseAid listing for the Caduet drug offered from Pfizer Laboratories Div Pfizer Inc. This Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Pfizer Laboratories Div Pfizer Inc
NON-PROPRIETARY NAME: amlodipine besylate and atorvastatin calcium
SUBSTANCE NAME: AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2004-01-30
END MARKETING DATE: 0000-00-00


Caduet HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCaduet from Pfizer Laboratories Div Pfizer Inc
LABELER NAME: Pfizer Laboratories Div Pfizer Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 10(mg/1; mg/1)
START MARKETING DATE: 2004-01-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0069-2150_6722a493-1a03-49cb-8541-136acc657033
PRODUCT NDC: 0069-2150
APPLICATION NUMBER: NDA021540

Other AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Greenstone LLCAmlodipine besylate and Atorvastatin calcium
Mylan Pharmaceuticals Inc.Amlodipine besylate and atorvastatin calcium
Pfizer Laboratories Div Pfizer IncCaduet
Ranbaxy Pharmaceuticals Incamlodipine besylate and atorvastatin calcium