Tobramycin Injection, Solution
Product Images NDC 63323-306

5 FDA label images from Fresenius Kabi Usa, Llc · 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 Tobramycin (NDC 63323-306). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Nomogram (Nomogram)

Nomogram (Nomogram)
A reduced dosage nomogram chart showing the relationship between serum creatinine (mg/100 mL) on the x-axis and percent of normal dosage from Table 3 on the y-axis. Creatinine clearance (mL/min/1.73 m²) is also indicated along the top axis, ranging from 0 to 70.*
FDA Label Image

Logo (Premier Newr)

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of tobramycin showing its molecular arrangement with multiple amino and hydroxyl groups in a detailed skeletal formula.*
FDA Label Image

Tray (Tob Tray)

Tray (Tob Tray)
Label for Tobramycin Injection USP, 40 mg/mL (80 mg per 2 mL). The product is intended for intramuscular or intravenous use, must be diluted before use, and comes in a 25 x 2 mL multiple dose vial. It is labeled by Fresenius Kabi USA, LLC with NDC 63323-306. The label includes storage instructions and inactive ingredients information.*
FDA Label Image

Vial (Tob Vial)

Vial (Tob Vial)
Label for Tobramycin Injection USP 80 mg per 2 mL (40 mg/mL), a multiple dose vial for intramuscular or intravenous use. The label notes the product must be diluted before IV use and references usual dosage information on the package. Manufactured by Fresenius Kabi USA, LLC, with NDC 63323-306-26.*

* 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.