Sertraline Hydrochloride
Product Images NDC 16590-457

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sertraline Hydrochloride (NDC 16590-457). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stat Rx Usa 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

4e30d1b4-figure-01 (4e30d1b4 Figure 01)

Chemical structure of sertraline hydrochloride showing its molecular arrangement with two chlorine atoms attached to a phenyl ring and an amine hydrochloride group.*

FDA Label Image

Label Image 100 mg (Sertraline 100mg Label)

Label for Sertraline Hydrochloride 100 mg tablets, 90 count, distributed by STAT Rx USA LLC in Gainesville, GA. It is a generic product for Zoloft. The label includes the NDC 16590-416-90 and identifies Camber Pharma, Inc., Piscataway, NJ as the manufacturer. The label also includes dosage storage instructions and a caution about possible side effects, advising medication be taken with plenty of water.*

FDA Label Image

Label Image 25 mg (Sertraline 25mg Label)

Label for Sertraline hydrochloride tablets, 25 mg strength, containing 30 tablets per package. The product is generic for Zoloft and labeled by STAT Rx USA LLC in Gainesville, GA. Each tablet contains sertraline HCl equivalent to 25 mg sertraline. Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ. The label includes NDC codes 16590-700-30 and 31722-212-30, with lot and discard date information. A caution about dizziness and not taking medication with plenty of water is also shown.*

FDA Label Image

Label Image 50 mg (Sertraline 50mg Label)

Sertraline 50mg tablets, 90 count, labeled as generic for Zoloft. Packaged and distributed by STAT Rx USA LLC, Gainesville, GA. The label includes NDC 16590-457-90, manufacturing information by Camber Pharm., Inc., and warnings about drowsiness or dizziness advising to take with plenty of water. Marked as a sample with lot and discard date 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.