Celexa Tablet, Film Coated
Product Images NDC 0456-4020

4 FDA label images from Allergan, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Celexa (NDC 0456-4020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allergan, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Celexa 01

Celexa 01
Chemical structure diagram of citalopram hydrobromide, the active ingredient in Celexa tablets. The structure shows the molecular arrangement including aromatic rings, a nitrile group, and the hydrobromide salt form.*
FDA Label Image

Celexa 02

Celexa 02
The label for Celexa 10 mg film-coated tablets features the proprietary name Celexa and the generic name citalopram. It indicates a package containing 100 tablets, each with a strength equivalent to 10 mg of citalopram. The label includes storage instructions, cautionary notes for pharmacists, and states Allergan USA, Inc. as the labeler.*
FDA Label Image

Celexa 03

Celexa 03
Celexa 20 mg film-coated tablets packaging label. The label shows the brand name Celexa with the generic name citalopram, dosage form as tablets, and strength of 20 mg. The package contains 100 tablets. The labeler is Allergan, Inc., Madison, NJ. Additional storage and dispensing instructions are visible on the right side of the label.*
FDA Label Image

Celexa 04

Celexa 04
Label for Celexa 40 mg film-coated tablets, containing citalopram. The label states 100 tablets per container and is manufactured by Allergan, Inc. Dosage form is oral tablets. It includes storage instructions and medication guide dispensing information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.