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)

FDA Label Image

Norepinephrinecontainerlabel (Norepinephrinecontainerlabel)

Norepinephrinecontainerlabel (Norepinephrinecontainerlabel)
This is a description of Norepinephrine Bitartrate Injection, USP, which is a medication with a concentration of 4 mg/4 mL (1 mg/mL) used for intravenous infusion only. The warning on the label mentions the presence of sulfites. Each mL contains norepinephrine bitartrate, USP equal to 1 mg. The vial is a 4 mL single-dose vial and should be diluted before use, with the unused portion to be discarded. The medication should be protected from light and has an expiration date (MM/YYYY) provided. Manufactured by Aspiro Pharma Limited in India for Camber Pharmaceuticals, Inc., with manufacturing license number 36/MD/AP2013/FI6 in Piscataway, NJ 08854.*
FDA Label Image

Norepinephrinestructure (Norepinephrinestructure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.