Norepinephrine Bitartrate
Product Images NDC 72078-002

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norepinephrine Bitartrate (NDC 72078-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Carton Np

Norepinephrine Bitartrate Injection, USP by Mylan Institutional LLC. The label indicates 4 mg/4 mL (1 mg per mL) strength, supplied as 10 single-dose vials of 4 mL each. It is for intravenous infusion only, with warnings to dilute before use, discard unused portion, and protect from light. The label mentions it contains sulfites and provides storage and handling instructions.*

FDA Label Image

Vial

Label for Norepinephrine Bitartrate Injection, USP by Mylan Institutional LLC, showing strength of 4 mg per 4 mL (1 mg/mL). It is a sterile, single-dose vial intended for intravenous infusion only. The label includes warnings about sulfites, instructions to dilute before use, and protection from light. Manufacturer information and barcode are also visible.*

FDA Label Image

Vial 4 mg (Image 01)

Chemical structure of norepinephrine bitartrate showing the molecular arrangement of norepinephrine combined with the bitartrate moiety and water of hydration.*

FDA Label Image

Infusion Label

This is a partial text panel from an infusion label for Norepinephrine bitartrate by Mylan Institutional LLC. It includes fields to record the concentration (mg added to mL), the volume of solution, the rate of infusion in mL per minute, and the infusion start time.*

* 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.