CADUETamlodipine besylate, atorvastatin calcium

FDA approved the original new drug application for CADUET on January 30, 2004, sponsored by PHARMACIA. FDA’s record shows no approved efficacy supplement on the application since.

Application

NDA021540

Sponsor

PHARMACIA

Original approval

January 30, 2004

Review

standard review

Submission class

Type 4 - New Combination

Active ingredient

amlodipine besylate, atorvastatin calcium

Browse every approval whose brand starts with C, or the complete response letters FDA has published — the applications it did not approve.

Products under this application

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

FDA’s record shows no approved efficacy supplement on this application.

FDA records other approved supplements on this application, by the class code it assigns them: Labeling 28 · Manufacturing (CMC) 3. Those are changes to the label or to how the drug is made rather than new clinical evidence, so they are counted here and not listed.

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

Other approvals to PHARMACIA

• March 25, 2003SOMAVERTBLA021106
• August 24, 1995GENOTROPIN PRESERVATIVE FREEBLA020280
• February 21, 1992MAXAQUINNDA020013