Norepinephrine Bitartrate Injection, Solution, Concentrate
Product Images NDC 71288-439

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Norepinephrine Bitartrate (NDC 71288-439). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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

Package Label Principal Display Panel Norepinephrine Bitartrate Injection Usp Carton (Norepi Carton)

Packaging label for Norepinephrine Bitartrate Injection, USP 4 mg per 4 mL (1 mg per mL) concentrate for intravenous infusion. The box indicates 10 single-dose vials of 4 mL each. It includes usage warnings, storage instructions, and manufacturer information for Meitheal Pharmaceuticals Inc. and Kindos Pharmaceuticals Co., Ltd. The label features a barcode and NDC 71288-439-05.*

FDA Label Image

Structure (Norepi Straucture)

Chemical structure of norepinephrine bitartrate, showing the molecular arrangement of norepinephrine linked with bitartrate and a water molecule.*

FDA Label Image

Package Label Principal Display Panel Norepinephrine Bitartrate Injection Usp Vial Label (Norepi Vial)

Label for Norepinephrine Bitartrate Injection USP, 1 mg/mL (4 mg per 4 mL) concentrate solution for intravenous infusion. The label indicates a 4 mL single-dose vial, for intravenous use only. Manufactured by Meitheal Pharmaceuticals Inc., Chicago, IL, made in China, with directions to dilute before use and protect from light.*

* 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.