Naproxen Sodium Tablet
Product Images NDC 62207-728

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Naproxen Sodium (NDC 62207-728). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Ltd, 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

62207 327 41 Carton

The image shows the packaging label for Naproxen Sodium Tablets USP 220 mg by Granules India Limited. It contains 24 film-coated tablets. The label highlights the product as a pain reliever/fever reducer for headache pain and states the strength lasts up to 12 hours. It includes a barcode and mentions that it contains no gluten-containing grains.*

FDA Label Image

62207 327 41 Label

Drug Facts panels for Naproxen Sodium Tablets USP 220 mg film-coated tablets by Granules India Limited. The text provides active ingredient info, uses, warnings, directions, and additional drug facts for this NSAID pain reliever and fever reducer. Key warnings cover allergy, stomach bleeding, and pediatric use advice. Instructions include dosage limits, storage, and when to ask a doctor or pharmacist. Includes inactive ingredients and contact details for questions.*

FDA Label Image

62207 328 51 Carton

Naproxen Sodium Tablets USP 220 mg film-coated tablets packaging label. The label indicates the product is an NSAID for headache pain relief, with strength to last 12 hours. It contains 10 caplet-shaped tablets per package. Manufactured by Granules India Limited in Hyderabad, India. The label also includes a barcode and storage instructions.*

FDA Label Image

62207 328 51 Label

Drug Facts text panel for Naproxen Sodium Tablets USP 220 mg, a nonsteroidal anti-inflammatory drug (NSAID) used as a pain reliever and fever reducer, containing no gluten ingredients. The label details uses, warnings including allergy alert and stomach bleeding risks, directions for use, storage instructions, and inactive ingredients. It also includes manufacturer information for Granules India Limited.*

FDA Label Image

62207 728 24 Carton

The image shows the packaging label for Naproxen Sodium Tablets USP, with a strength of 220 mg. It is a film-coated tablet indicated as an NSAID for back and muscle pain relief. The label states the product is manufactured by Granules India Limited and contains 24 tablets. It also highlights the duration of effect as up to 12 hours and includes various drug facts, warnings, active ingredients, and usage instructions.*

FDA Label Image

62207 728 24 Label

Drug Facts label panels for Naproxen Sodium Tablets USP 220 mg film-coated tablets by Granules India Limited. The label includes active ingredient information, uses, warnings, directions for use, and other drug facts. It details pain relief uses, possible side effects, proper dosage instructions, and storage information. The label also cautions about allergies, stomach bleeding risk, and advises consultation with a doctor or pharmacist before use.*

FDA Label Image

62207 729 24 Carton

Packaging label for Naproxen Sodium Tablets USP 220 mg, a film-coated tablet used as a pain reliever/fever reducer. The label indicates 24 caplets (capsule-shaped tablets) per package and states the product is manufactured by Granules India Limited in Hyderabad, India. The label highlights the product strength, non-gluten content, and includes drug facts, warnings, directions, and a barcode.*

FDA Label Image

62207 729 24 Label

Drug Facts panels for Naproxen Sodium Tablets USP 220 mg film-coated tablets by Granules India Limited. The panels list active ingredient details, uses for pain relief and fever reduction, warnings including allergy and stomach bleeding risks, directions, and other information such as inactive ingredients and storage instructions.*

FDA Label Image

62207 761 24 Carton

Packaging label for Naproxen Sodium Tablets USP 220 mg, a film-coated tablet and nonsteroidal anti-inflammatory drug (NSAID) used as a pain reliever/fever reducer. The label shows it contains 24 tablets, manufactured by Granules India Limited, made in India. It includes warnings, drug facts with active ingredient details, directions, and storage instructions. The label notes the product contains no gluten-containing grains and highlights strength to last 12 hours.*

FDA Label Image

62207 761 24 Label

Drug Facts panels for Naproxen Sodium Tablets USP 220 mg, detailing active ingredient, purposes, uses, warnings, directions, and other safety information. The text covers pain relief, fever reduction, allergy warnings, stomach bleeding risk, and guidelines for use in adults and children, including specific precautions and inactive ingredients. Manufactured by Granules India Limited, the label also references the product as equivalent to Aleve tablets.*

FDA Label Image

62207 762 24 Carton

Packaging label for Naproxen Sodium Tablets USP 220 mg film-coated tablets, a nonsteroidal anti-inflammatory drug (NSAID). The label indicates it is a pain reliever/fever reducer, produced by Granules India Limited, Hyderabad, India. The package contains 24 caplets and states no gluten-containing ingredients. Additional drug facts, directions, warnings, and contact information are printed on the unfolded carton.*

FDA Label Image

62207 762 24 Label

Drug Facts text panels for Naproxen Sodium Tablets USP 220 mg by Granules India Limited. The panels display active ingredient information, uses, warnings including allergy and stomach bleeding risks, directions for use, potential side effects, and storage instructions. It also includes specific warnings for heart attack, stroke, and allergic reactions, and advises consulting a doctor or pharmacist before use.*

* 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.