Ibu Tablet
Product Images NDC 71610-275

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibu (NDC 71610-275). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 800 mg (71610 0275 60)

IBU 800 mg oral tablets prescription label from Aphena Pharma Solutions - Tennessee, LLC. The label states Ibuprofen, USP, with a 90-tablet bottle. It includes storage instructions between 20-25°C, mentions dispensing in a tight light-resistant container, and cautions to keep out of reach of children. Manufactured by Elder's Laboratories Louisiana, LLC in Shreveport, LA. The label also displays lot number, NDC code 71610-0275-60, and expiration date in 2021.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Strucuture (Structure)

Chemical structure of ibuprofen, showing its molecular arrangement with a benzene ring substituted by isobutyl and propionic acid groups.*

FDA Label Image

Table (Table)

This table categorizes adverse reactions reported with IBU (Ibuprofen) tablets by incidence and causal relationship. It lists gastrointestinal, central nervous system, dermatologic, special senses, hematologic, metabolic/endocrine, cardiovascular, allergic, renal, and miscellaneous events, dividing them into incidence greater than 1% but less than 3%, precise incidence unknown with probable causal relationship, and precise incidence unknown with causal relationship unknown.*

* 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.