Escitalopram Oxalate
Product Images NDC 33261-955

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 33261-955). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals Llc, 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

1 (Escitalopram 20mg Tab For Torrent 1)

1 (Escitalopram 20mg Tab For Torrent 1)
This is a table showing the Treatment-Emergent Adverse Reactions observed with frequencies greater than 2% and greater than placebo for major depressive disorder. The table shows the percentage of patients experiencing various adverse reactions while taking Escitalopram Oxalate (N=715) compared to Placebo (N=592). Some of the common adverse reactions included dry mouth, diarrhea, insomnia, and ejaculation disorder. The text also includes notes about the denominators used for males and females.*
FDA Label Image

2 (Escitalopram 20mg Tab For Torrent 2)

FDA Label Image

1 (Escitalopram 20mg Tab For Torrent 3)

FDA Label Image

1 (Escitalopram 20mg Tab For Torrent 4)

FDA Label Image

Image Label (Escitalopram 20mg Tab For Torrent 5)

Image Label (Escitalopram 20mg Tab For Torrent 5)
This is a description of a medication containing Escitalopram, which is manufactured by Aidarex Pharmaceuticals LLC and Torrent Pharmaceuticals Ltd. It comes in the form of film-coated tablets and is available in 20mg dosages. The medication is commonly used to treat depression and anxiety. There is no further information available.*

* 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.