Phenobarbital Sodium Injection
Product Images NDC 42494-442

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 Phenobarbital Sodium (NDC 42494-442). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cameron 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

Chemical Structure (Phenobarbital 01)

Chemical Structure (Phenobarbital 01)
Chemical structure of phenobarbital sodium, depicting the molecular arrangement including a phenyl group, ethyl group, and sodium salt component relevant to the active ingredient in Phenobarbital Sodium injection products.*
FDA Label Image

Principal Display Panel (65 mg/mL Vial Label)

Principal Display Panel (65 mg/mL Vial Label)
Phenobarbital Sodium Injection USP 65 mg/mL label for intramuscular or slow intravenous use. The label indicates 25 single-dose 1 mL vials, storage at controlled room temperature (20°-25°C), and warns against use if discolored or containing precipitate. The label includes NDC 42494-441-25 and is manufactured for Novaplus by Cameron Pharmaceuticals.*
FDA Label Image

Principal Display Panel (130 mg/mL Vial Label)

Principal Display Panel (130 mg/mL Vial Label)
Phenobarbital Sodium Injection, USP 130 mg/mL label for intramuscular or slow intravenous use. The package contains 25 single-dose 1 mL vials. Manufactured for Novaplus by Cameron Pharmaceuticals. Storage instructions and warnings about discoloration or precipitate on the label.*

* 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.