Lexapro
Product Images NDC 16590-139

3 FDA label images from Stat Rx Usa Llc · 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 Lexapro (NDC 16590-139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stat Rx Usa 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

Lexapro 10mg Label Image (Lexapro 10mg Label 16590 139)

Lexapro 10mg Label Image (Lexapro 10mg Label 16590 139)
Lexapro 10 mg oral tablet packaging label showing 30 tablets. The label includes the NDC number 16590-139-30 and identifies the active ingredient as Escitalopram Oxalate, equivalent to 10 mg Escitalopram. The product is packaged and distributed by STAT Rx USA LLC in Gainesville, GA, and manufactured by Foresd Pharm., Inc. in St. Louis, MO. The label includes a prescription-only warning and disposal instructions.*
FDA Label Image

Lexapro 5mg Label Image (Lexapro 5mg Label 16590 833)

Lexapro 5mg Label Image (Lexapro 5mg Label 16590 833)
LEXAPRO 5 mg tablet bottle label with 45 tablets, labeled as a generic for escitalopram oxalate equivalent to 5 mg escitalopram. Distributed by STAT Rx USA LLC in Gainesville, GA. Manufacturer is Forest Pharm., Inc., St. Louis, MO. The label includes cautions about medication use and storage instructions along with NDC numbers and lot information.*
FDA Label Image

Structural Formula (Lex00 0008 01)

Structural Formula (Lex00 0008 01)
Chemical structure of the active ingredient in Lexapro, showing the molecular formula arrangement including chlorine (Cl), fluorine (F), and a side chain with nitrogen (N) atoms. An ethanol molecule (C2H6O) is also indicated.*

* 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.