Sertraline Hydrochloride
Product Images NDC 13107-012

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 13107-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurolife Pharma 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

Package Label.principal Display Panel (25 mg(100's Bottle))

This is information about a medication named Sertraline Hydrochloride contained in tablet form. The tablets contain Sertaline hydrochloride equivalent to 25 my senraine. Usual Dosage information is provided along with storage instructions. The medication is manufactured by Aurolife Pharma LLC and distributed by Aurobindo Pharma USA, Inc. A medication guide is provided separately. No additional details are available.*

FDA Label Image

Package Label.principal Display Panel (50 mg(100's Bottle))

Each tablet in this medication contains 0.5 mg of Sertraline hydrochloride. It is recommended to store the medication at a temperature range of 20°-25°C (68°-77°F) with excursions permitted at a temperature range of 15°-30°C (59°-86°F). No further information is available.*

FDA Label Image

Package Label.principal Display Panel (100 mg(100's Bottle))

These are Sertraline Hydrochloride Tablets containing 2100 mg of Sertraline each. They are recommended for storage at a temperature of 20-25°C. The usual dosage is to be determined by the accompanying prescribing information. These tablets were manufactured by Aurolife Pharma LLC for Aurobindo Pharma USA Inc. The batch number is not legible.*

FDA Label Image

Sertraline Structure (Sertraline Str)

* 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.