Tobramycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 72266-163

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tobramycin (NDC 72266-163). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fosun Pharma Usa 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

Carton Label (Tobramycin Carton Label)

Packaging label for Tobramycin injection, USP, 1.2 grams per vial, in powder form for lyophilized solution for intravenous use. The label displays NDC 72266-163-06 and indicates a package of 6 vials. Manufactured by Fosun Pharma USA Inc, the label warns this pharmacy bulk package is not for direct infusion.*

FDA Label Image

Vial Label (Tobramycin Container Label)

Label for Tobramycin for Injection, USP 1.2 grams per vial, a lyophilized powder for intravenous use. The label indicates it is a pharmacy bulk package not for direct infusion, distributed by Fosun Pharma USA Inc. It includes usage instructions, storage conditions, and manufacturer information stating the product is made in India.*

FDA Label Image

Tobramycin-nomogram (Tobramycin Nomogram)

A line graph showing a reduced dosage nomogram for Tobramycin injection, relating percent of normal dosage from Table 3 to serum creatinine levels (mg/100 mL) and creatinine clearance (mL/min/1.73 m²). The graph depicts a decreasing linear relationship where dosage percentage reduces as serum creatinine increases or creatinine clearance decreases.*

FDA Label Image

Tobramycin-structure (Tobramycin Structure)

Chemical structure of the active ingredient Tobramycin, showing its molecular arrangement with multiple amine (NH2) and hydroxyl (OH) groups attached to its sugar rings.*

* 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.