Ibuprofen And Famotidine Tablet, Film Coated
Product Images NDC 80425-0422

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ibuprofen And Famotidine (NDC 80425-0422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of 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

Ibuprofen/famotidine 800mg-26.6mg #30 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 01)

Ibuprofen/famotidine 800mg-26.6mg #30 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 01)
Label for ibuprofen and famotidine 800 mg / 26.6 mg film-coated tablets, prescription only, packaged by Advanced Rx of Tennessee, LLC in Nashville, TN. The label includes storage instructions, comparison to a reference product due to DUEXIS, NDC 80425-0422-01, lot and expiration date fields, and a barcode. The package count is 30 tablets.*
FDA Label Image

Ibuprofen/famotidine 800mg-26.6mg #60 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 02)

Ibuprofen/famotidine 800mg-26.6mg #60 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 02)
Label for Ibuprofen and famotidine 800 mg / 26.6 mg film-coated tablets by Advanced Rx of Tennessee, LLC. The label shows storage instructions, a barcode, numbering (#60), and expiration date of 6/30/2025. It includes an instruction not to transfer the drug to others and references a comparison to Duexis. The label is for prescription use only.*
FDA Label Image

Ibuprofen/famotidine 800mg-26.6mg #90 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 03)

Ibuprofen/famotidine 800mg-26.6mg #90 (Ibuprofen Famotidine 800mg 26.6mg 80425 0422 03)
Label for Ibuprofen and famotidine 800 mg / 26.6 mg tablet, film-coated, oral dosage form. The product is packaged by Advanced Rx of Tennessee, LLC, Nashville, TN, with a storage recommendation of 20°-25°C (68°-77°F). The label mentions lot and expiration date information and states that the medication is for prescription use only. The label also includes comparison information referencing Duexis with associated NDC numbers and barcodes.*
FDA Label Image

Famotidine-structure (Ibuprofen Famotidine Structure)

Famotidine-structure (Ibuprofen Famotidine Structure)
Chemical structure of famotidine, one of the active ingredients in the Ibuprofen and famotidine combination drug product. The molecular arrangement shows nitrogen, sulfur, carbon, and other atoms connected by various bonds.*
FDA Label Image

Ibuprofen-structure (Ibuprofen Structure)

Ibuprofen-structure (Ibuprofen Structure)
Chemical structure diagram showing the molecular structure of the active ingredient Ibuprofen, including its isobutyl group attached to a benzene ring and a carboxylic acid functional group.*

* 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.