Ibuprofen And Famotidine Tablet, Film Coated
Product Images NDC 85509-1010

View Photos of 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 Ibuprofen And Famotidine (NDC 85509-1010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Rx 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 And Famotidine 800 mg/26.6 mg Tablets (30count)

Ibuprofen And Famotidine 800 mg/26.6 mg Tablets (30count)
Label for Ibuprofen and famotidine Tablets, 800 mg/26.6 mg, containing 30 film-coated tablets. The product is Rx only, manufactured by Alkem Laboratories Ltd., and repackaged by Phoenix Rx LLC, Hatboro, PA. Storage instructions and barcode with QR codes for package insert and prescribing information are visible.*
FDA Label Image

39aa00d8 4a83 E53a E063 6394a90af248

39aa00d8 4a83 E53a E063 6394a90af248
Oval, white film-coated tablet imprinted with 'iF 826' on one side. This is a prescription tablet form of Ibuprofen and famotidine as labeled by PHOENIX RX LLC.*
FDA Label Image

Famotidine-structure (Ibuprofen Famotidine Structure)

Famotidine-structure (Ibuprofen Famotidine Structure)
Chemical structure diagram of famotidine, showing its molecular arrangement with labeled atoms and bonds. This structure represents one of the active ingredients in the Ibuprofen and famotidine oral tablet product by PHOENIX RX LLC.*
FDA Label Image

Ibuprofen-structure (Ibuprofen Structure)

Ibuprofen-structure (Ibuprofen Structure)
Chemical structure diagram depicting the molecular arrangement of ibuprofen, showing its aromatic ring and side chains as part of the compound.*

* 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.