Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 50090-7830

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 50090-7830). 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

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Chemical structure of Sertraline Hydrochloride, showing its molecular framework including a bicyclic ring system and chlorinated aromatic ring, with an attached NHCH3 hydrochloride group.*
FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets in a blister pack. The tablets are round, light yellow, and embossed with an identifying code. The blister card contains 10 tablets arranged in two rows of five. The product is labeled by A-S Medication Solutions for oral use.*
FDA Label Image

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Sertraline Hydrochloride 50 mg film-coated tablets packaged in a blister pack with multiple round tablets, each marked with a 'D' imprint. The blister pack is silver with a clear plastic cover exposing the tablets. No other text or branding is visible in the image.*
FDA Label Image

Label Image (Lbl500907830)

Label Image (Lbl500907830)
Sertraline Hydrochloride 50 mg film-coated tablets label from A-S Medication Solutions. The bottle label displays the product name, strength, quantity of 90 tablets, and storage instructions to keep at 68 to 77 degrees Fahrenheit. The label includes the NDC 50090-7830 and package lot number.*

* 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.