Sertraline Hydrochloride
Product Images NDC 58118-0834

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 58118-0834). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, 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

Sertraline 50

Sertraline 50mg Tablets label from Clinical Solutions Wholesale, LLC, showing a package quantity of 30 tablets. The label includes the NDC number 58118-0834-8, manufacturer details (Pola USA, Inc., Miami, FL), a barcode, and batch and manufacturing information with a September 2021 manufacture date.*

FDA Label Image

Image (Eca3f504 92e3 4765 B175 23cdcaf20634 01)

Chemical structure diagram of sertraline hydrochloride showing its molecular framework including two chlorine atoms and an N-methylamine hydrochloride group.*

FDA Label Image

Sertraline 25mg Tablet 30 Count Blister Card (Image 01)

Label for Sertraline 25 mg tablets by Clinical Solutions Wholesale, LLC. Includes NDC 58118-0833-8, manufacturer Cipla USA, Inc., lot number SAMPLE123, batch number SAMPLE456, and manufacturing date October 2018. The label shows a quantity of 30 tablets and storage instructions to store at 20° to 25°C (68° to 77°F).*

FDA Label Image

Sertraline 100mg Tablet 30 Count Blister Card (Image 03)

Label for Sertraline Hydrochloride 100 mg tablets by Clinical Solutions Wholesale, LLC, repackaged from Cipla USA. The label includes NDC 58118-0835-8, manufacturing and batch details, and storage instructions for room temperature. The package quantity is 30 tablets.*

* 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.