Norepinephrine Bitartrate Injection, Solution, Concentrate
Product Images NDC 31722-372

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norepinephrine Bitartrate (NDC 31722-372). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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
FDA Label Image

Norepinephrinecartonlabel (Norepinephrinecartonlabel)

Norepinephrinecartonlabel (Norepinephrinecartonlabel)
Carton label for Norepinephrine Bitartrate Injection, USP 1 mg/mL (4 mg/4 mL) by Camber Pharmaceuticals, Inc., containing 10 single-dose vials of 4 mL each. The label states it is for intravenous infusion only, includes dilution instructions, storage temperature, warnings about sulfites, and manufacturing details including a U.S. contact number.*
FDA Label Image

Norepinephrinecontainerlabel (Norepinephrinecontainerlabel)

Norepinephrinecontainerlabel (Norepinephrinecontainerlabel)
Label for Norepinephrine Bitartrate Injection, USP, 4 mg/4 mL (1 mg/mL) concentrate solution for intravenous infusion. The product is a 4 mL single-dose vial manufactured by Aspiro Pharma Limited, India, and labeled for Camber Pharmaceuticals, Inc. The label includes usage instructions, dosage strength, barcode, and placeholders for lot number and expiration date.*
FDA Label Image

Norepinephrinestructure (Norepinephrinestructure)

Norepinephrinestructure (Norepinephrinestructure)
Chemical structure of norepinephrine bitartrate monohydrate, depicting the norepinephrine molecule complexed with bitartrate and one molecule of water (monohydrate).*

* 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.