Gentamicin Injection, Solution
Product Images NDC 70518-4757

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gentamicin (NDC 70518-4757). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm1 (Gentamicin 80mg 2ml (40mg mL) 70518 4757 00)

Gentamicin Injection Sterile 40 mg/mL solution in 2 mL vials with a total of 25 vials per package. The label states the strength as 80 mg per 2 mL. It is intended for intramuscular or intravenous use and must be diluted for intravenous use. Manufactured by RemedyRepack Inc., Indiana, PA, with the NDC number 70518-4757-00. The vial stopper is not made with natural rubber latex. Storage instructions advise keeping the medication at 20-25°C with allowed excursions to 15-30°C.*

FDA Label Image

Remedy_label (Remedy Label)

Gentamicin Injection 40 mg/mL sterile solution vial, containing 2 mL (80 mg total). The label indicates it is for intramuscular or intravenous use and must be diluted for intravenous use. It is a multiple-dose vial, not made with natural rubber latex. Labeler is RemedyRepack Inc., Indiana, PA. The vial has NDC 70518-4757-01 and includes storage instructions and a warning about potential toxicity of aminoglycosides.*

FDA Label Image

Gentamicin-structure (Gentamicin Str)

Chemical structure of gentamicin showing the molecular components and the variants C1, C2, and C1A. The diagram includes the gentamicin molecule linked to sulfuric acid (XH2SO4).*

* 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.