Escitalopram Tablet, Film Coated
Product Images NDC 70518-4239

5 FDA label images from Remedyrepack Inc. · 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 (NDC 70518-4239). 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

Image (69cff3b0 F256 46a1 B0bf 055d27dd945e 01)

FDA Label Image

Mm1 (Escitalopram 20mg 70518 4239 00)

FDA Label Image

Mm2 (Escitalopram 20mg 70518 4239 01)

FDA Label Image

Mm3 (Escitalopram 20mg 70518 4239 02)

FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for escitalopram 20 mg film-coated tablets in a quantity of 30 tablets. The label includes the NDC number 70518-4239-00 and indicates the manufacturer as RemedyRepack Inc., repackaged from Rising Pharma, Inc. It cautions to keep medication out of children's reach and directs users to the package insert for use directions.*

* 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.