Tobramycin Injection
Product Images NDC 68083-241

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tobramycin (NDC 68083-241). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Tobramycin-spl-carton-label (Tobramycin Spl Carton Label)

Label for Tobramycin Injection USP, 2 g per 50 mL (40 mg per mL), Pharmacy Bulk Package by Gland Pharma Limited. The label states it is for intravenous use, must be diluted before IV use, and is not for direct infusion. The package contains a 50 mL vial and includes storage instructions and a barcode.*

FDA Label Image

Tobramycin-spl-container-label (Tobramycin Spl Container Label)

Label for Tobramycin Injection USP 2 g per 50 mL (40 mg per mL) intravenous injection, pharmacy bulk package, not for direct infusion. The 50 mL vial is labeled for dilution prior to use and includes instructions and warnings. Manufactured by Gland Pharma Limited, India. NDC 68083-241-01.*

FDA Label Image

Tobramycin-spl-figure (Tobramycin Spl Figure)

A reduced dosage nomogram chart for Tobramycin injection displaying the relationship between serum creatinine (mg/100 mL) on the X-axis and percent of normal dosage from table on the Y-axis. It includes a top axis showing creatinine clearance (mL/min/1.73 m²). The plot consists of a single diagonal line indicating dosage adjustment based on creatinine levels.*

FDA Label Image

Tobramycin-spl-structure (Tobramycin Spl Structure)

Chemical structure of Tobramycin, showing its molecular connectivity including multiple amino and hydroxyl groups across its ring structures.*

* 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.