Penicillin G Potassium Injection, Powder, For Solution
Product Images NDC 83634-103

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 Penicillin G Potassium (NDC 83634-103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avenacy 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

Figure (Pen0e 0000 01)

Figure (Pen0e 0000 01)
Chemical structure of penicillin G potassium, showing its molecular framework with functional groups characteristic of penicillin antibiotics, including a beta-lactam ring and potassium salt moiety.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL – Vial Label)

Package Label (PRINCIPAL DISPLAY PANEL – Vial Label)
Label for Buffered Penicillin G Potassium injection, USP, 5,000,000 units per vial by Avenacy Inc. The label highlights intramuscular or intravenous use and provides detailed drug content and storage instructions, including unit amounts per mL and sterile storage conditions.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL – Vial Label)

Package Label (PRINCIPAL DISPLAY PANEL – Vial Label)
Label for Penicillin G Potassium injection, USP, 20,000,000 units per vial (20 million units per vial) in powder form for solution, intended for intravenous infusion only. The label states it is buffered, preservative-free, nonpyrogenic, and contains potassium equivalent to 10,000 units penicillin G as G salt. The manufacturer is Avenacy Inc., with storage recommendations noted to keep refrigerated at or below 8°C. The label includes barcode, lot and expiration date fields, and dilution volume guidelines.*

* 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.