Sertraline Hydrochloride Tablet, Film Coated
Product Images NDC 50090-7700

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 50090-7700). 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 configuration including a bicyclic core with a chlorine-substituted phenyl ring and an amine hydrochloride functional group.*

FDA Label Image

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Sertraline Hydrochloride 100 mg film-coated tablets blister pack, oral dosage form. The pack includes individual tablets sealed in a clear plastic and foil blister. The labeler is A-S Medication Solutions. The packaging is designed for outpatient prescription use.*

FDA Label Image

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Sertraline Hydrochloride 100 mg film-coated tablets are shown in a white plastic bottle with a child-resistant cap. The label displays the brand and generic name, strength, dosage form, and oral route. The product is manufactured by A-S Medication Solutions. The bottle is designed for prescription use, consistent with the NDC 50090-7700.*

FDA Label Image

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Sertraline Hydrochloride 100 mg film-coated tablets package label from A-S Medication Solutions. The label indicates each tablet contains sertraline hydrochloride USP equivalent to 100 mg of sertraline. The package contains 30 tablets. Storage instructions specify 20 to 25 degrees Celsius. The product NDC is 50090-7700.*

* 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.