Mesnex Injection, Solution
Product Images NDC 83703-559

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Mesnex (NDC 83703-559). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bamboo Us Bidco Lcc, 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

Representative Vial Label 1g 0338-1305-01 (Image 01)

Label for Mesnex (mesna) Injection 1 g vial, an intravenous solution for human prescription drug use. The label shows the brand and generic name, strength, route, and includes storage and manufacturing information from Bamboo US Bidco LLC.*

FDA Label Image

Representative Carton Label 1g 0338-1305-01 1 Of 4 (Image 02)

MESNEX (mesna) Injection 1 g per vial label for intravenous use. The multidose vial is manufactured by Baxter Healthcare Corporation, Deerfield, IL. Label includes NDC 0338-1305-01 and indicates prescription use only.*

FDA Label Image

Representative Carton Label 1g 0338-1305-01 2 Of 4 (Image 03)

Packaging label panel for MESNEX mesna injection, solution by Baxter Healthcare Corporation. The label includes handling instructions indicating the product is fragile and should be stored at controlled room temperature between 20° to 25°C (68° to 77°F), with permitted excursions to 15° to 30°C (59° to 86°F). The label references USP standards and provides manufacturer location in Deerfield, IL, USA.*

FDA Label Image

Representative Carton Label 1g 0338-1305-01 3 Of 4 (Image 04)

MESNEX (mesna) Injection 1g per vial label for intravenous use. The label shows it is manufactured by Baxter Healthcare Corporation, Deerfield, IL, and includes a lot/expiration date section and barcode. This vial contains a single multidose 1g injection.*

FDA Label Image

Representative Carton Label 1g 0338-1305-01 4 Of 4 (Image 05)

Text panel from a MESNEX (mesna) injection solution label describing concentration, composition, preservative content, usage directions, and manufacturing information. It specifies each vial contains 1 g mesna in 10 mL water with additional components to adjust pH, includes a preservative, and cautions use only with thorough knowledge of dosing and indications. Manufactured by Baxter Healthcare Corporation in Deerfield, IL, USA, made in Germany.*

FDA Label Image

Representative Box Label 1g Panel 1 Of 4 (Image 06)

MESNEX (mesna) Injection 1 g multidose vial label for intravenous use. Each vial contains 1 g mesna in 10 mL water as a sterile, nonpyrogenic solution. The label includes handling and storage instructions, manufacturer information (Baxter Healthcare Corporation, made in Germany), and a barcode. The product is Rx only.*

FDA Label Image

Representative Box Label 1g Panel 2 Of 4 (Image 07)

Packaging label for MESNEX mesna injection, 100 mg/mL, in a 10 mL multidose vial. The label highlights the product name MESNEX and specifies it is for intravenous use, provided by Bamboo US Bidco LCC. The label features a vertical red stripe with white text on a white background.*

FDA Label Image

Representative Box Label 1g Panel 3 Of 4 (Image 08)

Label for MESNEX (mesna) Injection 1 g per vial, a sterile intravenous solution. The label states each vial contains 1 g mesna in 10 mL water with preservatives and instructions for storage at 20°-25°C. Manufactured by Baxter Healthcare Corporation, Deerfield, Illinois, USA, made in Germany. The package includes 10 multidose vials.*

FDA Label Image

Representative Box Label 1g Panel 4 Of 4 (Image 09)

MESNEX 100 mg/mL injection solution label for intravenous use. The label indicates the product is supplied in 10 multidose vials, labeled by Bamboo US Bidco LCC with the NDC 83703-559. The design includes a red vertical bar with the product name and concentration.*

* 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.