Norepinephrine Solution
Product Images NDC 81298-9658

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norepinephrine (NDC 81298-9658). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Long Grove Pharmaceuticals, 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

Figure (Nor0r 0000 01)

Chemical structure of norepinephrine bitartrate showing the norepinephrine molecule and its associated bitartrate and water components.*

FDA Label Image

Principal Display Panel – 4 mg Pouch Label (Nor0r 0000 02)

Label for Norepinephrine Injection 4 mg per 250 mL (16 mcg/mL) in 0.9% Sodium Chloride, solution for intravenous use. The single-dose container is manufactured by Long Grove Pharmaceuticals, LLC. Label includes storage instructions, usage warnings, and a barcode.*

FDA Label Image

Principal Display Panel – 8 mg Pouch Label (Nor0r 0000 03)

Label for Norepinephrine 32 mcg/mL (8 mg per 250 mL) intravenous solution in 0.9% Sodium Chloride Injection provided in a 250 mL single-dose container. The label shows usage instructions for intravenous infusion and storage conditions, including keeping the product in sealed overwrap until use. Manufactured for Long Grove Pharmaceuticals, LLC.*

FDA Label Image

Principal Display Panel – 16 mg Pouch Label (Nor0r 0000 04)

Label for Norepinephrine solution in 0.9% Sodium Chloride Injection, 64 mcg/mL strength, packaged in a 250 mL container. The label includes directions for intravenous infusion, storage conditions, and handling instructions. The product is manufactured by Long Grove Pharmaceuticals, LLC.*

* 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.