Naproxen Sodium Tablet, Film Coated
Product Images NDC 43063-909

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Naproxen Sodium (NDC 43063-909). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

43063909 Label (43063909)

43063909 Label (43063909)
This is a drug facts label for Naproxen Sodium tablets, which are a pain reliever/fever reducer that are also formulated to temporarily relieve minor aches and pains due to arthritis, muscular aches, backache, menstrual cramps, headache, toothache, and the common cold. It is important to note that taking more than the directed amount of this medication can cause severe stomach bleeding and therefore, people with allergies to aspirin should avoid using this medication. The warning also applies to people who have a history of stomach problems such as heartburn, any blood-clotting or bleeding disorder, heart disease, high blood pressure, liver or kidney disease, asthma, or had a stroke. Pregnant or breastfeeding women should consult their doctors before taking this medication, and they should avoid using it during the first three months of pregnancy unless directed by a physician. Additionally, each tablet contains sodium 21 mg, and the recommended dose for adults and children 12 years and older is one tablet to be taken every 8 to 12 hours while symptoms last, but the smallest effective dose should be taken to avoid harmful effects. Furthermore, the label includes the NDC number, lot number, and expiration date, and reveals that the medication is marketed and packaged by PD-Rx Pharmaceuticals Inc, Oklahoma City, OK 73127.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.