Bivalirudin Injection, Powder, Lyophilized, For Solution
Product Images NDC 55150-210

View Photos of 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 Bivalirudin (NDC 55150-210). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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

Package Label-principal Display Panel (250 mg per vial)

Package Label-principal Display Panel (250 mg per vial)
Label for Bivalirudin injection, powder, lyophilized, for solution, 250 mg per vial. The label states intravenous use, single-dose vial, and discarding unused portion. Distributed by AuroMedics Pharma LLC. Storage conditions and vial contents details are included.*
FDA Label Image

Package Label-principal Display Panel (250 mg per vial)

Package Label-principal Display Panel (250 mg per vial)
Packaging label for Bivalirudin for Injection, 250 mg per vial. The label indicates the product is for intravenous use only and contains 10 single-dose vials. The labeler is Auromedics Pharma LLC. Storage and usage instructions are included, along with the NDC number 55150-210-10.*
FDA Label Image

Bivalirudin Trifluoroactetate Chemical Structure (Bivalirudin Str)

Bivalirudin Trifluoroactetate Chemical Structure (Bivalirudin Str)
Chemical structure diagram of bivalirudin, depicting its peptide backbone with various amino acid residues and side chains, including multiple amide and carboxyl groups. The structure illustrates the complex linear arrangement characteristic of this peptide anticoagulant drug.*

* 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.