Citalopram Tablet
Product Images NDC 70518-2617

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 70518-2617). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Citalopram 20mg 70518 2617 01

Citalopram 20mg 70518 2617 01
The text provides information about the medication Citalopram which is available only with a prescription. It includes details such as NDC number, expiration date, lot number, and the manufacturer's information. The medicine should be kept out of reach of children and stored at a temperature range of 20-26°C (63-77°F) with a permission of excursions up to 15-30°C (59-86°F). The package insert should be checked for directions of use. Moreover, the medication was repackaged by RemedyRepack Inc. located in Indiana, USA.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Citalopram is a prescription-only medication manufactured by Cipla USA, Inc. The medication is stored between 20-26°C and should be kept away from children. The package insert should be consulted for directions for use. The medication has an NDC number of 70518-2617-00, and a source NDC number of 63097-0823-07. There is also a lot number and an expiration date not included in the text. The medication has been repackaged by RemedyRepack Inc. located in Indiana, PA.*
FDA Label Image

Structure

* 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.