Cefuroxime Axetil For Oral Suspension
Product Images NDC 63304-963

3 FDA label images from Ranbaxy Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cefuroxime Axetil For Oral Suspension (NDC 63304-963). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ranbaxy 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

Label001 (Label001)

Label001 (Label001)
Label for Cefuroxime Axetil For Oral Suspension, USP 125 mg/5 mL by Ranbaxy Pharmaceuticals Inc. The 100 mL reconstituted suspension is for oral use only and requires prescription. The label includes instructions for reconstitution, storage conditions, and warnings to shake well before use and discard after 10 days.*
FDA Label Image

Label002 (Label002)

Label002 (Label002)
Label for Cefuroxime Axetil For Oral Suspension, USP by Ranbaxy Pharmaceuticals Inc. It shows a strength of 250 mg/5 mL in a 50 mL bottle when reconstituted. The label includes usage instructions, storage conditions, and indicates the product is Rx only. The NDC code 63304-964-03 is displayed prominently along with a barcode.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of the active ingredient in Cefuroxime Axetil For Oral Suspension by Ranbaxy Pharmaceuticals Inc, showing the molecular arrangement including a beta-lactam ring and other functional groups characteristic of this antibiotic prodrug.*

* 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.