Bivalirudin Injection, Powder, Lyophilized, For Solution
Product Images NDC 71288-427

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 71288-427). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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

Structural Formula (Biv05 0000 01)

Structural Formula (Biv05 0000 01)
Chemical structure diagram of bivalirudin showing the peptide sequence and side chains, illustrating the molecular composition of the active pharmaceutical ingredient bivalirudin.*
FDA Label Image

Principal Display Panel – Bivalirudin For Injection 250 mg Carton (Bival Viz Carton)

Principal Display Panel – Bivalirudin For Injection 250 mg Carton (Bival Viz Carton)
Packaging label for BIVALIRUDIN 250 mg per vial injection, a lyophilized powder for solution, for intravenous use. The label shows the brand Novaplus, with storage instructions and formulation details. It is labeled for Meitheal Pharmaceuticals Inc. and includes the NDC 71288-427-92. The container is sterile and preservative-free, marked for single-dose vial use only.*
FDA Label Image

Principal Display Panel – Bivalirudin For Injection 250 mg Vial Label (Bival Viz Vial)

Principal Display Panel – Bivalirudin For Injection 250 mg Vial Label (Bival Viz Vial)
Label for Bivalirudin injection 250 mg per vial, lyophilized powder for intravenous solution. The single-dose vial contains 250 mg of bivalirudin. Labeler is Meitheal Pharmaceuticals Inc., Chicago, IL. Made in China. Novaplus is noted as the trademark.*

* 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.