Aspirin Tablet, Delayed Release
Product Images NDC 71679-301

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aspirin (NDC 71679-301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Health Pharma Usa, 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

3 (1000)

Packaging label for Health Pharma USA Adult Low Dose Aspirin 81 mg delayed-release tablets. The product is indicated as a pain reliever (NSAID) with a safety-coated aspirin regimen for safe pain relief. The label highlights 1000 enteric coated tablets in the package and includes warnings and directions for use. The label prominently displays the NDC 71679-301 along with manufacturer contact information.*

FDA Label Image

2 (500)

The image shows two Drug Facts panels for aspirin delayed-release tablets 81 mg by Health Pharma USA. It includes active ingredient details, uses for temporary relief of minor aches and pains, warnings about conditions like Reyes syndrome and stomach bleeding, directions for use, storage instructions, inactive ingredients, and contact information for questions or comments. It also emphasizes not to use if tamper-evident seal is broken or missing.*

FDA Label Image

1 (Label)

Text panel for Aspirin Delayed Release Tablets USP, 81 mg, describing batch, manufacturing, expiration details (unfilled), quantity of 135,000 tablets, and NDC number 71679-301-00. Includes warnings to keep out of reach of children and storage instructions at controlled room temperature. Notes the product is a bulk shipment for further processing by Health Pharma USA LLC and manufactured by Elysium Pharmaceuticals Ltd.*

* 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.