Ibu
Product Images NDC 43353-273

4 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibu (NDC 43353-273). 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 800mg (43353 273)

Bottle Label 800mg (43353 273)
Packaging label for IBU ibuprofen 800 mg in a carton containing 180 tablets. The label includes the NDC number 43353-0273-80, lists the manufacturer as Dr. Reddy's Laboratories Louisiana, LLC from Shreveport, LA, and states the product is for prescription use only. The product is repackaged by Aphena Pharma Solutions.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Strucuture (Structure)

Strucuture (Structure)
Chemical structure of ibuprofen showing the molecular arrangement including isobutyl and propionic acid functional groups attached to a benzene ring.*
FDA Label Image

Table (Table)

Table (Table)
A data table listing adverse reactions associated with IBU, categorized by frequency and probable causal relationship. The table is organized by system (e.g., gastrointestinal, central nervous system, dermatologic) with corresponding reactions grouped under incidence greater than 1% but less than 3%, precise incidence unknown with probable causal relationship, and precise incidence unknown with causal relationship unknown. Footnotes define the classification criteria for reactions.*

* 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.