Norepinephrine Bitartrate Injection, Solution
Product Images NDC 0338-0116

3 FDA label images from Baxter Healthcare Corporation · 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 Norepinephrine Bitartrate (NDC 0338-0116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Structural Formula (Image 01)

Structural Formula (Image 01)
Chemical structure diagram of norepinephrine bitartrate showing its molecular components and associated water of hydration.*
FDA Label Image

Norepinehrine Representative Container Label 0338-0112-20 (Image 02)

Norepinehrine Representative Container Label 0338-0112-20 (Image 02)
NOREPINEPHRINE BITARTRATE 4 mg/250 mL injection, solution in 5% dextrose for intravenous use, manufactured by Baxter Healthcare Corporation. The label includes dosage information, storage instructions, and handling precautions. The container is a VIAFLO single-dose 250 mL unit made in Ireland, with details on temperature storage and disposal.*
FDA Label Image

Representative Container Label 0338-0108-20 (Image 03)

Representative Container Label 0338-0108-20 (Image 03)
The label is for NORepinephrine Bitartrate in 5% Dextrose Injection, 8 mg per 250 mL solution for intravenous infusion. The label shows the text "Baxter" and indicates a 250 mL vial size. The product is manufactured by Baxter Healthcare Corporation, Deerfield, IL, made in Ireland. Storage and usage instructions are included on the label.*

* 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.