Naproxen Tablet, Delayed Release
Product Images NDC 71205-060

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naproxen (NDC 71205-060). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Description (0778e9f1 B341 448c Ba26 Cfa4370e8123 01)

Chemical structure of naproxen showing its molecular formula C14H14O3 and molecular weight 230.26. The structure includes a methoxy group and a carboxyl group (R=COOH) attached to a naphthalene backbone with indicated stereochemistry.*

FDA Label Image

Clinical Pahrmacology (0778e9f1 B341 448c Ba26 Cfa4370e8123 02)

A data table comparing pharmacokinetic parameters for Naproxen delayed-release tablets 500 mg twice daily versus Naproxen tablets 500 mg twice daily. It shows mean values with coefficient of variation for Cmax (peak concentration), Tmax (time to peak), and AUC0-12 hr (area under the curve) for both formulations.*

FDA Label Image

Dosage And Administration (0778e9f1 B341 448c Ba26 Cfa4370e8123 03)

A text panel showing dosage information for Naproxen delayed-release tablets, listing available strengths of 375 mg or 500 mg and instructions to take the tablet twice daily.*

FDA Label Image

71205-060-60 (0778e9f1 B341 448c Ba26 Cfa4370e8123 04)

Label for Naproxen EC 375 mg delayed-release tablets, 60 count, by Proficient Rx LP. The label shows the product name, strength, dosage form, and quantity. It includes manufacturing details by InvaGen Pharmaceuticals, storage instructions, and a medication guide advisory. The label features the NDC 71205-060-60 and is intended for prescription use only.*

* 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.