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Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 55154-4317
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 55154-4317). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Cardinal Health 107, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Structural Formula (E7476adc A940 4e76 A1dd C418de493bc0 02)
Chemical structure of diltiazem hydrochloride showing its molecular arrangement including ring structures, sulfur, oxygen, nitrogen atoms, and associated hydrochloride component.*
Bag Label (Image 01)
Label for Diltiazem Hydrochloride extended-release capsules, USP 120 mg. The label states a package size of 10 capsules and includes dosage and storage information. It shows the product is distributed by Cardinal Health and manufactured by TWi Pharmaceuticals. Additional warnings and instructions for institutional use are also provided.*
Bag Label (Image 02)
Diltiazem Hydrochloride extended-release capsules, USP 180 mg, in a 10-capsule unit dose package. Label includes storage instructions, dosage note, warnings, and manufacturing details from TWi Pharmaceuticals, with distribution by Cardinal Health. The packaging is intended for institutional use and is not child resistant.*
Bag Label (Image 03)
Diltiazem HCl Extended-Release Capsules, USP 240 mg label for a 10-capsule unit dose package. The label includes storage instructions, dosage information, warnings about child resistance, and manufacturer and distributor details including Cardinal Health 107, LLC. The product is an oral, extended-release capsule for prescription use.*
* 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.
