Escitalopram Tablet, Film Coated
Product Images NDC 70518-2317

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 70518-2317). 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

Escitalopram 20mg 70518 2317 01

Escitalopram 20 mg film-coated tablet label showing a quantity of 30 tablets. The label includes the product name, strength, dosage form, and the labeler RemedyRepack Inc. Directions advise referring to the package insert, with storage instructions and repackaging information visible. The NDC number 70518-2317-01 is present along with manufacturing details.*

FDA Label Image

Escitalopram 20mg 70518 2317 02

Label for Escitalopram 20 mg film-coated tablets, quantity 90, by RemedyRepack Inc. The label includes NDC number 70518-2317-02, storage instructions, and a QR code. It specifies the repackaging location in Indiana, PA, and warns to keep medication out of reach of children.*

FDA Label Image

Remedy_label (Remedy Label)

Escitalopram 20 mg film-coated tablets packaging label showing quantity of 30 tablets. The label includes the NDC 70518-2317-00, manufacturer Solco in Cranbury, NJ, and repackager RemedyRepack Inc. It states the drug is prescription only and provides storage instructions and a QR code.*

FDA Label Image

Structural Formula (Structure)

Chemical structure of Escitalopram, the active ingredient in this human prescription drug. The diagram shows the molecular structure including key rings and functional groups typical for Escitalopram, along with a notation indicating the presence of C2H6O4 (likely a salt or hydrate form).*

* 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.