Adakveo Injection
Product Images NDC 0078-0883

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Adakveo (NDC 0078-0883). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novartis Pharmaceuticals Corporation, 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

Preparation And Administration (Seg101 01)

Preparation And Administration (Seg101 01)
This text seems to be a formula for calculating the volume of a medication called ADAKVEO based on the patient's body weight and prescribed dose. However, some characters are unreadable making the formula incomplete and its functionality not available.*
FDA Label Image

Principal Display Panel Ndc 0078-0883-61 Rx Only Adakveo® (crizanlizumab-tmca) Injection 100 mg/10 mL (10 mg/ml) For Intravenous Infusion After Dilution. 1 Single-dose Vial. Discard Unused Portion. Novartis (Seg101 02)

Principal Display Panel Ndc 0078-0883-61 Rx Only Adakveo® (crizanlizumab-tmca) Injection 100 mg/10 mL (10 mg/ml) For Intravenous Infusion After Dilution. 1 Single-dose Vial. Discard Unused Portion. Novartis (Seg101 02)
ADAKVEO is an injection medication used for intravenous infusion after dilution. Each 10 mL vial contains 100 mg of crizanlizumab-tmca, citric acid, poloxamer 188, sodium citrate, sucrose, and water for injection. Before using the injection, ensure that there is no acceleration or particular matter. It is recommended to store and transport the vial refrigerated at 2°C to 8°C (36°F to 46°F) while protected from light. For more information, please visit their website or call as indicated.*

* 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.