Aphexda Injection, Powder, Lyophilized, For Solution
Product Images NDC 82737-073

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Aphexda (NDC 82737-073). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biolinerx Usa 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

Carton Label (Carton)

Aphexda 62 mg per vial injection label for motixafortide. The lyophilized powder for solution is intended for subcutaneous injection. The label includes storage instructions to keep refrigerated at 2°C to 8°C, directions for reconstitution, and states it is for healthcare provider use only. Manufactured for BioLineRx Ltd and made in the USA, the label also features NDC 82737-073-01 and a barcode.*

FDA Label Image

Citimage (Cit)

Chemical structure of Motixafortide, the active ingredient in Aphexda. The diagram shows the molecular configuration with labeled atoms and bonds representative of Motixafortide's chemical composition.*

FDA Label Image

Fbaimage (Fba)

Chemical structure of Motixafortide, illustrating its molecular framework with specific atoms and bonds arranged in a defined pattern.*

FDA Label Image

Nalimage (Nal)

Chemical structure of Motixafortide, the active ingredient in Aphexda, a human prescription drug injection in lyophilized powder form for subcutaneous use. The image depicts the molecular structure with various atoms and bonds represented.*

FDA Label Image

Sequence (Sequence)

Chemical structure diagram of Motixafortide, showing its sequence composition and molecular arrangement as a peptide with labeled amino acid components.*

* 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.