Sertraline Hydrochloride
Product Images NDC 50090-2976

4 FDA label images from A-s Medication Solutions · 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 50090-2976). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500902609)

Label Image (Lbl500902609)
Label for Sertraline Hydrochloride 100 mg tablets by A-S Medication Solutions, Libertyville, IL. It includes the NDC number 50090-2609-0 and the product number 5819-0. Contains 30 tablets with storage instructions to keep between 68-77 degrees Fahrenheit. Contains sertraline hydrochloride equivalent to 100 mg sertraline per tablet.*
FDA Label Image

Lbl500902976

Lbl500902976
Sertraline Hydrochloride 25 mg bottle label from A-S Medication Solutions showing NDC 50090-2976-0. The label states each tablet contains sertraline hydrochloride USP equivalent to 25 mg sertraline, with storage instructions at 68 to 77 degrees Fahrenheit. Package size is 30 tablets.*
FDA Label Image

Lbl500903089

Lbl500903089
Label of Sertraline Hydrochloride 50 mg tablets, packaged by A-S Medication Solutions. The label shows the product number 5818-2, lot number, and that the package contains 90 tablets. The active ingredient is sertraline hydrochloride USP, 50 mg strength.*
FDA Label Image

Chemical Structure (Sertraline Str)

Chemical Structure (Sertraline Str)
Chemical structure of sertraline hydrochloride showing the molecular arrangement including chlorine atoms and the amine hydrochloride group.*

* 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.