Dantrolene Sodium Capsule
Product Images NDC 68084-300

4 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dantrolene Sodium (NDC 68084-300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Ahp30021

Ahp30021
Dantrolene Sodium 25 mg oral capsule is shown here. The capsule is half yellow and half green, with the imprint "G441" printed on the yellow and green halves. The capsule is manufactured by American Health Packaging.*
FDA Label Image

Blister

Blister
Dantrolene Sodium 25 mg oral capsules packaging label from American Health Packaging. The label indicates the drug is a peripheral skeletal muscle relaxant. It includes lot number 123456 and expiry date 07/21. Multiple identical labels are shown on a perforated sheet for individual capsule packaging.*
FDA Label Image

Carton

Carton
Label for Dantrolene Sodium Capsules, USP 25 mg, oral tablets indicated as a peripheral skeletal muscle relaxant. The label shows a 30-capsule count (3 bottles of 10 capsules each), with NDC 68084-300-21. The product is distributed by American Health Packaging, Columbus, Ohio. The label includes usage, storage instructions, and warnings about prescription status and child safety.*
FDA Label Image

Structure

Structure
Chemical structure of the active ingredient Dantrolene Sodium, depicting its molecular arrangement including nitrobenzene, furan, and hydantoin rings with sodium and water 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.