Penicillin G Potassium Injection, Powder, For Solution
Product Images NDC 25021-153

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 25021-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Structural Formula (Pen0d 0001 01)

Structural Formula (Pen0d 0001 01)
Chemical structure diagram of penicillin G potassium showing the arrangement of its atoms and bonds as part of its molecular structure.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Pen0d 0001 02)

Package Label – Principal Display Panel – Vial Label (Pen0d 0001 02)
Label for Penicillin G Potassium injection, USP, 5,000,000 units per vial by Sagent Pharmaceuticals. The label indicates this is a buffered, powder for solution for injection, available for intramuscular or intravenous use. It includes dosage unit details, reconstitution instructions, and storage conditions.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Pen0d 0001 03)

Package Label – Principal Display Panel – Vial Label (Pen0d 0001 03)
Label for Penicillin G Potassium for Injection, USP, 20,000,000 units per vial powder for intravenous infusion. The label includes dosage form as injection powder, administration route intravenous, and manufacturer Sagent Pharmaceuticals. It also specifies that the product is sterile, preservative-free, nonpyrogenic, and contains natural rubber latex 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.