Ibu Tablet
Product Images NDC 66267-963

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibu (NDC 66267-963). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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.

FDA Label Image

Pdp (66267 963 00 D55)

Label for IBU Ibuprofen 800 mg Tablets from NuCare Pharmaceuticals, Inc. The label shows the NDC number 66267-963-00, lot number, expiration date, and indicates a package size of 100 tablets. It states 'Rx Only' and includes instructions to see the manufacturer's label for a full list of ingredients. The label also features storage warnings and manufacturer information.*

FDA Label Image

Strucuture (Structure)

Chemical structure of ibuprofen, showing its molecular framework with characteristic aromatic ring and functional groups.*

FDA Label Image

Table (Table)

A table listing adverse reactions reported with IBU (Ibuprofen) 800 mg oral tablets by NuCare Pharmaceuticals, Inc. It categorizes reactions by body system and incidence rate: greater than 1% but less than 3%, probable causal relationship, and precise incidence unknown. Systems covered include gastrointestinal, central nervous, dermatologic, special senses, hematologic, metabolic/endocrine, cardiovascular, allergic, renal, and miscellaneous.*

* 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.