Escitalopram Tablet, Film Coated
Product Images NDC 80425-0320

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 80425-0320). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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

Description (Description)

Chemical structure diagram of escitalopram, illustrating its molecular composition including a fluorophenyl group connected to a bicyclic ring system and an amino group side chain, along with an associated molecule of ethanol (C2H6O).*

FDA Label Image

Label 1 (Escitalopram 10mg 80425 0320 01)

The label for Escitalopram 10 mg film-coated tablets, packaged by Advanced Rx Pharmacy of Tennessee, LLC in Nashville, TN. The label states the strength (10 mg), tablet form, and storage instructions (20°-25°C). It notes the package contains 30 tablets and includes a comparison to LEXAPRO with corresponding NDC numbers, lot number placeholder, and expiration date 8/4/2025. The label also shows a barcode and Solco Healthcare information with a serial number.*

FDA Label Image

Label 2 (Escitalopram 10mg 80425 0320 02)

Escitalopram 10 mg film-coated tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions, comparison to Lexapro, NDC 80425-0320, lot number, expiration date 8/4/2025, and manufacturer Solco Healthcare. The package contains 60 tablets.*

FDA Label Image

Label 3 (Escitalopram 10mg 80425 0320 03)

Escitalopram 10 mg tablet film coated packaging label with quantity #90, distributed by Advanced Rx Pharmacy of Tennessee, LLC in Nashville, TN. The label states storage conditions at 20-25°C (68-77°F) and includes a comparison to Lexapro with associated NDC numbers and expiration date of 8/4/2025. The label also features barcodes and tracking 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.