Pentobarbital Sodium Injection, Solution
Product Images NDC 25021-676

3 FDA label images from Sagent Pharmaceuticals · 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 Pentobarbital Sodium (NDC 25021-676). 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 (Pen03 0007 01)

Structural Formula (Pen03 0007 01)
Chemical structure of pentobarbital sodium depicted as a heterocyclic ring with multiple side chains, including ethyl and isopropyl groups, and corresponding atomic bonds labeled with standard chemical notation.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Pen03 0007 02)

Package Label – Principal Display Panel – Vial Label (Pen03 0007 02)
Label for Pentobarbital Sodium Injection, USP, 50 mg/mL (1,000 mg per 20 mL) in a multi-dose vial. The label shows administration routes as intravenous or intramuscular, with a caution that it is not for subcutaneous use. The label includes lot and expiration details, and identifies Sagent Pharmaceuticals as the manufacturer.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Pen03 0007 03)

Package Label – Principal Display Panel – Vial Label (Pen03 0007 03)
Label of pentobarbital sodium injection, USP, 2,500 mg per 50 mL (50 mg/mL) solution in a 50 mL multi-dose vial. The label indicates intramuscular and intravenous use, includes caution against subcutaneous administration, and notes preservative-free, sterile, nonpyrogenic solution. Manufactured by Sagent Pharmaceuticals.*

* 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.