Naproxen And Esomeprazole Magnesium Tablet, Delayed Release
Product Images NDC 85509-1438

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naproxen And Esomeprazole Magnesium (NDC 85509-1438). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Rx 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

Label (85509 1438 3)

Label for Naproxen and Esomeprazole Magnesium delayed-release tablets, 500 mg naproxen and 20 mg esomeprazole, oral tablets. The label indicates 30 tablets per bottle, Rx only, manufactured by ScieGen Pharmaceuticals, Inc. and repackaged by PHOENIX RX LLC, Hatboro, PA. It includes dosage instructions, storage conditions, and warnings.*

FDA Label Image

Figure1 (Figure1)

A line graph showing the concentration of Esomeprazole and Naproxen over time (24 hours). The left y-axis measures Esomeprazole concentration in ng/mL, peaking early and then declining rapidly to near zero by about 8 hours. The right y-axis measures Naproxen concentration in µg/mL, rising gradually to a peak around 6-8 hours and then slowly decreasing through 24 hours. The x-axis represents time in hours.*

FDA Label Image

Structure1 (Structure1)

Chemical structure of naproxen, one of the active ingredients in the naproxen and esomeprazole magnesium delayed-release tablets by Phoenix RX LLC.*

FDA Label Image

Structure2 (Structure2)

Chemical structure of the active ingredient esomeprazole magnesium, shown as a dimer complexed with magnesium ion (Mg2+) and three water molecules.*

* 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.