Tobramycin Injection
Product Images NDC 67457-428

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tobramycin (NDC 67457-428). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Structural Formula (Image 01)

Chemical structure of Tobramycin, illustrating its molecular arrangement with rings and functional groups consistent with the aminoglycoside antibiotic.*

FDA Label Image

Serum Creatinine (Image 02)

A line graph titled 'REDUCED DOSAGE NOMOGRAM' showing the relationship between serum creatinine levels (mg/100 mL) on the x-axis and percent of normal dosage from Table 3 on the y-axis. The graph plots a single linear line indicating dosage adjustments based on creatinine clearance.*

FDA Label Image

30 mL Carton (Image 03)

Packaging label for Tobramycin Injection USP 1.2 g/30 mL (40 mg/mL) by Mylan Institutional LLC. The label indicates the product is sterile for intramuscular or intravenous use and requires dilution for IV use. The package contains 10 multi-dose vials of 30 mL each. The label includes storage instructions and usage information.*

FDA Label Image

2 mL Carton (Image 04)

Packaging label for Tobramycin Injection, USP 80 mg/2 mL (40 mg/mL) sterile injection by Mylan Institutional LLC. The label indicates the product is for intramuscular or intravenous use and must be diluted for IV use. The package contains 25 multi-dose vials of 2 mL each. The label lists active and inactive ingredients, storage instructions, and manufacturer details.*

* 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.