Tromethamine Injection, Solution
Product Images NDC 71357-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tromethamine (NDC 71357-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Milla Pharmaceuticals 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

Image Description (Tromethamine Inj 500ml Bottle Label)

Image Description (Tromethamine Inj 500ml Bottle Label)
Label for Tromethamine Injection 500 mL solution, containing 3.6 g tromethamine per 100 mL, distributed by Milla Pharmaceuticals Inc. The label states the product is sterile, nonpyrogenic, for intravenous use, and to store at 20 to 25°C. It includes lot number P4166 and expiration date June 2027, along with barcodes and Milla Pharmaceuticals logo.*
FDA Label Image

Image Description (Tromethamine Inj 500ml Carton Label)

Image Description (Tromethamine Inj 500ml Carton Label)
Label for Tromethamine Injection 3.6 g/100 mL solution in a 500 mL single-dose container. The label includes product details such as pH adjustment, solute concentration, usage instructions for intravenous administration, and storage conditions. Distributed by Milla Pharmaceuticals Inc., the label also features a barcode and manufacturing details indicating Made in Italy.*
FDA Label Image

Image Description (Tromethamine Inj Structure)

Image Description (Tromethamine Inj Structure)
Chemical structure of Tromethamine, depicting its molecular arrangement with hydroxymethyl groups and an amino group attached to the central carbon atom.*

* 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.