Plerixafor Injection, Solution
Product Images NDC 31722-373

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Plerixafor (NDC 31722-373). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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
FDA Label Image

Plerixaforinjcartonlabel (Plerixaforinjcartonlabel)

Plerixaforinjcartonlabel (Plerixaforinjcartonlabel)
Plerixafor Injection, USP 24 mg/1.2 mL (20 mg/mL) subcutaneous injection label from Camber Pharmaceuticals, Inc. The label indicates a single-dose vial with no preservatives, specifying storage instructions and manufacturer details including HETERO LABS LIMITED in India. The NDC is 31722-373-31, with dosing and administration information referenced to the package insert.*
FDA Label Image

Plerixaforinjstructure (Plerixaforinjstructure)

Plerixaforinjstructure (Plerixaforinjstructure)
Chemical structure diagram of the active ingredient plerixafor, showing interconnected nitrogen-containing ring systems and a benzene ring in the molecular framework.*
FDA Label Image

Plerixaforinjviallabel (Plerixaforinjviallabel)

Plerixaforinjviallabel (Plerixaforinjviallabel)
Label for Plerixafor Injection, USP 24 mg/1.2 mL (20 mg/mL) single-dose vial by Camber Pharmaceuticals, Inc. The label shows the NDC 31722-373-31, subcutaneous injection use, and batch coding area. Manufactured by HETERO Labs Limited, India.*

* 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.