Norepinephrine Bitartrate
Product Images NDC 70121-1576

3 FDA label images from Amneal Pharmaceuticals Llc · 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 70121-1576). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal 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.

Product Images & Figures Index

FDA Label Image

1 (Norepinephrine Bitartrate Injection Usp 1)

1 (Norepinephrine Bitartrate Injection Usp 1)
Chemical structure of norepinephrine bitartrate, illustrating the molecular components including the norepinephrine moiety and the bitartrate salt with associated water of hydration.*
FDA Label Image

1 (Norepinephrine Bitartrate Injection Usp 2)

1 (Norepinephrine Bitartrate Injection Usp 2)
Label for Norepinephrine Bitartrate Injection, USP 4 mg/4 mL (1 mg/mL) by Amneal Pharmaceuticals LLC. It is for intravenous infusion only, contains sulfites, and is provided in a 4 mL single-dose vial. The label includes storage instructions, dilution directions, manufacturer and distributor information, a barcode, and spaces for lot number and expiration date.*
FDA Label Image

1 (Norepinephrine Bitartrate Injection Usp 3)

1 (Norepinephrine Bitartrate Injection Usp 3)
Norepinephrine Bitartrate Injection, USP 4 mg/4 mL (1 mg/mL) sterile injection by Amneal Pharmaceuticals LLC. The packaging contains 10 single-dose vials of 4 mL each. The label includes warnings about dosage control, sulfite content, and instructions to dilute before use. It also provides storage information and manufacturer details, with NDC 70121-1576-7 clearly shown.*

* 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.