Caffeine Citrate Injection
Product Images NDC 51754-0500

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Caffeine Citrate (NDC 51754-0500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Exela Pharma Sciences, Llc, 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

Structure (Image 01)

Structure (Image 01)
Chemical structure of caffeine citrate showing the molecular formula C14H18N4O9 and molecular weight 386.31.*
FDA Label Image

Exela Logo (Image 02)

FDA Label Image

Logo (Image 03)

FDA Label Image

Vial Label_injection (Image 04)

Vial Label_injection (Image 04)
Caffeine Citrate Injection, USP label for intravenous use, 60 mg per 3 mL (20 mg/mL) strength. The single-dose vial contains 3 mL of sterile, nonpyrogenic caffeine citrate injection. The label includes dosage instructions, storage conditions, and manufacturer information from Exela Pharma Sciences, LLC. It is marked Rx only with NDC 51754-0500-1.*
FDA Label Image

Carton_injection (Image 05)

Carton_injection (Image 05)
Packaging label for Caffeine Citrate Injection, USP 60 mg/3 mL (20 mg/mL) intravenous injection by Exela Pharma Sciences, LLC. The label states it is for single use only with a 3 mL single dose vial. Storage instructions and dosage information are included. The NDC is 51754-0500-1 and the label indicates the product is sterile, nonpyrogenic, and preservative-free.*

* 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.