Bivalirudin Injection, Solution
Product Images NDC 70511-142

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 70511-142). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Maia 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

Bivalirudin-spl-10packcarton (Bivalirudin Spl 10packcarton)

Bivalirudin-spl-10packcarton (Bivalirudin Spl 10packcarton)
Bivalirudin Injection 250 mg/50 mL (5 mg/mL) single-dose vials packaging label. The label indicates the product is for intravenous use only, ready to use, and should not be diluted. Pack contains 10 single-dose vials. Labeler is MAIA Pharmaceuticals, Inc. Includes usage, storage instructions, bar code, and manufacturing information.*
FDA Label Image

Bivalirudin-spl-chemical-structure (Bivalirudin Spl Chemical Structure)

Bivalirudin-spl-chemical-structure (Bivalirudin Spl Chemical Structure)
Chemical structure diagram of bivalirudin, showing its amino acid sequence and peptide bonds in a linear form with labeled residues.*
FDA Label Image

Bivalirudin-spl-monocarton (Bivalirudin Spl Monocarton)

Bivalirudin-spl-monocarton (Bivalirudin Spl Monocarton)
Bivalirudin Injection 250 mg/50 mL (5 mg/mL) in a single-dose vial for intravenous use. The label states 'Ready To Use, Do Not Dilute' and instructs to discard unused portions. Manufactured for MAIA Pharmaceuticals, Inc. The label includes storage instructions, recommended dosage reference, and contains product barcode and revision date 03/2024.*

* 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.