Sertraline Hydrochloride
Product Images NDC 52959-872

4 FDA label images from H.j. Harkins Company Inc. · 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 52959-872). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company Inc., 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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4e30d1b4-figure-01 (4e30d1b4 Figure 01)
Chemical structure of Sertraline Hydrochloride, showing its molecular framework with two chlorine atoms attached to a benzene ring and a methylamino group.*
FDA Label Image

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Sertraline HCL 25 mg tablet label showing lot number STT00QE, manufacturer CAMBER PHM located in Hauppauge, NY, and expiration date 02/11. The label indicates light green film-coated tablets and references Zoloft with NDC 31722-212-05. It includes typical caution and usage instructions, product quantity (#60), and repackaging information by H.J. Harkins Company Inc.*
FDA Label Image

4e30d1b4-figure-03 (4e30d1b4 Figure 03)

4e30d1b4-figure-03 (4e30d1b4 Figure 03)
Label for Sertraline Hydrochloride 50 mg tablets, manufactured by Camber Pharmaceuticals. The label includes lot number SRT06QE, expiration 12/11, and indicates the product is light blue film-coated tablets. It compares the product to Zoloft and provides handling warnings and a dosage instruction advisory to follow doctor directions or see outer packaging. The label also shows multiple identical smaller labels with the same product details and a quantity of 60 tablets each.*
FDA Label Image

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4e30d1b4-figure-04 (4e30d1b4 Figure 04)
Label for Sertraline Hydrochloride 100 mg tablets, manufactured by Cambier Pharma and labeled by H.J. Harkins Company Inc. The label includes batch number SRL105QE, expiration date 05/11, and compares the product to Zoloft. It identifies the tablets as light yellow film-coated and provides a warning to take as directed by a doctor, with usual dosage information on the outer packaging. Multiple smaller label segments repeat key product details and lot information.*

* 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.