Naproxen
Product Images NDC 51655-626

View Photos of 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 Naproxen (NDC 51655-626). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Pharmaceuticals, 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

51655-626-20 (51655 626 20)

51655-626-20 (51655 626 20)
Naproxen 500 MG tablet carton label showing 20 tablets for prescription use only. The label includes NDC numbers, lot number NW50310007, and expiration date 08/2016. It provides storage instructions and mentions Glenmark Generics Ltd and Northwind Pharmaceuticals as manufacturer and distributor. Dosage advice refers to package insert.*
FDA Label Image

51655-626-25 (51655 626 25)

51655-626-25 (51655 626 25)
Naproxen 500 MG tablet bottle label by Northwind Pharmaceuticals, LLC with a count of 60 tablets. The label includes the product NDC 51655-626-25, lot number NW50310008, and expiration date 08/2016. Storage instructions specify keeping tablets between 68-77 degrees F, protected from moisture and out of reach of children. Additional manufacturing and distribution details are also provided.*
FDA Label Image

51655-626-83 (51655 626 83)

51655-626-83 (51655 626 83)
Naproxen 500 MG tablet bottle label from Northwind Pharmaceuticals, LLC. The label indicates 180 tablets, prescription only, lot number NW50310009, and expiration date August 2016. It includes storage instructions, dosage note to see package insert, and manufacturing and repackaging details.*
FDA Label Image

Naproxen 51655-626 (Naproxen 51655 626)

Naproxen 51655-626 (Naproxen 51655 626)
Naproxen Tablets 500 mg packaging label showing a container of 30 tablets. The label indicates prescription use only, lot number NW50310001, and an expiration date of January 2016. Manufactured by Glenmark Generics Ltd and relabeled by Northwind Pharmaceuticals, LLC. Storage instructions and dosage reference to medication guide are included.*

* 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.