Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 80425-0310

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 80425-0310). 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)

Description (Description)
Chemical structure of Sertraline Hydrochloride, showing a bicyclic framework with two chlorine atoms and a methylamine hydrochloride group attached.*
FDA Label Image

Label 1 (Sertraline HCl 100mg 80425 0310 01)

Label 1 (Sertraline HCl 100mg 80425 0310 01)
Sertraline Hydrochloride 100 mg tablet, film-coated, in a package showing labeler Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions, a comparison to Zoloft, the NDC 80425-0310-01, lot number, and expiration date 10/31/2025. It contains 30 tablets.*
FDA Label Image

Label 2 (Sertraline HCl 100mg 80425 0310 02)

Label 2 (Sertraline HCl 100mg 80425 0310 02)
Sertraline Hydrochloride 100 mg film-coated tablets packaging label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions, lot number, expiration date (10/31/2025), and a note comparing the product to Zoloft. The package contains 60 tablets.*
FDA Label Image

Label 3 (Sertraline HCl 100mg 80425 0310 03)

Label 3 (Sertraline HCl 100mg 80425 0310 03)
Sertraline HCL 100 mg tablet packaging label by Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions at 20-25°C (68-77°F), a barcode, lot number, expiration date of 10/31/2025, comparison to Zoloft, and manufacturer details as Aurobindo Pharm. Label shows a NDC of 80425-0310.*

* 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.