Naproxen Tablet
Product Images NDC 25000-138

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Naproxen (NDC 25000-138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marksans Pharma Limited, 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

Naprox 250mg 1000s Bottle Label

FDA Label Image

Naprox 250mg 30s Bottle Label

Each tablet of NDC 25000-138-03 contains Naproxen, USP 250 mg. It is a prescribed medicine with instructions to see the package insert for full prescribing information. The tablet must be kept in a light-resistant container, and the seal under the cap must not be broken or missing. The tablets have to be stored at 20°-25°C (68°-77°F) excursions permitted to mg 15°-30°C (59°-86°F). The tablets are manufactured by Marksans Pharma Ltd. The given information seems to be related to a description of a medication.*

FDA Label Image

Naprox 375mg 1000s Bottle Label

This is a medication package of Naproxen, USP 375mg manufactured by Marksans Pharma Ltd. The package contains 1000 tablets with dimensions of 140 x 60 mm. It is advisable to refer to the package insert for full prescribing information. The tablets should be stored at a temperature between 20°C-25°C (68°F-77°F) with excursions permitted to 15°C-30°C (59°F-86°F). It's mandatory to keep it in a tamper-evident and light-resistant container. Pharmacists should dispense the medication with the provided medication guide separately for each patient. The package was manufactured for Time-Cap Labs Inc. and has information in PANTONE 485 C, PANTONE 300 C M, PANTONE 273 C, B PANTONE 254 C, BB Black.*

FDA Label Image

Naprox 375mg 30s Bottle Label

This is a prescription drug containing Naproxen, USP 375 mg. The drug should be stored at 20°-25°C (68°-77°F) with excursions permitted to 15°-30°C (59°-86°F). Dispensing should be done in a light-resistant container defined by USP. The package insert provides full prescribing information. The drug is manufactured for Time-Cap Labs, Inc. and manufactured by Marksans Pharma Ltd. The details of the lot are given, i.e., Plot No. L-82, L-83, Verna Indl. Estate, Verna, GOA - 403 722, India.*

FDA Label Image

Naprox 500mg 1000s Bottle Label

This is a product description for Naproxen tablets, which are a type of pain reliever. The tablets come in a tamper-evident container and contain 500mg of Naproxen USP. Customers should refer to the package insert for full dosage and usage instructions. The tablets are to be stored at room temperature, with permitted excursions to more extreme temperatures if necessary. The product should be dispensed in a light-resistant container as defined in USP. The tablets are manufactured by Marksans Pharma Ltd in Goa, India.*

FDA Label Image

Naprox 500mg 30s Bottle Label

This is a medication called UENOCHREN N with an active ingredient called Naproxen, USP 500 mg. It is a prescription drug dispensed in a light-resistant container with 30 tablets per container. It is manufactured for Time-Cap Labs, Inc. and manufactured by Marksans Pharma Ltd. Dispensing must be accompanied by the medication guide. Dosage and other relevant information can be found in the package insert. Store between 20°-25°C (68°-77°F) and do not use if seal under the cap is broken or missing. The lot number and expiration date are indicated on the package.*

FDA Label Image

Naprox Structure

FDA Label Image

Naprox Table

This text describes possible symptoms of a health problem that may include tiredness, weakness, diarrhea, itching, yellowing of the skin or eyes, stomach pain, flu-like symptoms, vomiting blood, bloody bowel movements, unusual weight gain, skin rash or blisters with fever, and swelling of the arms, legs, hands, and feet. It is important to seek medical attention if any of these symptoms occur.*

* 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.