Gentamicin Sulfate Injection, Solution
Product Images NDC 71872-7216

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Gentamicin Sulfate (NDC 71872-7216). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7216-1.pdp (71872 7216 1)

Label for Gentamicin Sulfate Injection USP 80 mg/2 mL (40 mg/mL) in a 2 mL single-dose Fliptop vial. The product is for intravenous or intramuscular use and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ. It includes caution and storage instructions, lot and expiration placeholders, and manufacturer details indicating it is made in Slovenia.*

FDA Label Image

Gentamicin Structural Formula (Gentamicin 01)

Chemical structure diagram of gentamicin, showing the core molecular structure with variations at the R group positions labeled as C1, C2, and C1A. The structure includes annotations for the sulfate (H2SO4) component.*

FDA Label Image

Novaplus Logo (Gentamicin 02)

FDA Label Image

Principal Display Panel (2 mL Vial Label)

Label for Gentamicin Sulfate Injection, USP 80 mg/2 mL (40 mg/mL as Gentamicin) single-dose vial. Indicated for intravenous or intramuscular use, requiring dilution for intravenous administration. Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. Proprietary name Gentamicin Sulfate Injection, solution dosage form with specified strength, highlighting dilution instructions and routes of administration.*

* 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.