Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 24979-182

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 24979-182). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, 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.

FDA Label Image

Diltiazem Hydrochloride Structural Formula (Image 01)

Chemical structure of diltiazem hydrochloride, illustrating its molecular components including aromatic rings, a thiazepine ring, a methoxy group, acetyl group, and hydrochloride salt.*

FDA Label Image

Diltiazem HCl Extended-release Capsules, Usp 60 mg Bottle Label (Image 02)

Label for Diltiazem HCl Extended-Release Capsules, USP 60 mg by Upsher-Smith Laboratories, LLC. The label shows vial packaging information for 100 capsules, oral route, with instructions to dispense in child-resistant containers and to keep out of reach of children. It includes storage conditions, manufacturer details, and a barcode with the National Drug Code (NDC) 24979-181-01. The dosage is indicated as twice-a-day.*

FDA Label Image

Diltiazem HCl Extended-release Capsules, Usp 90 mg Bottle Label (Image 03)

Label for Diltiazem HCl Extended-Release Capsules, USP, 90 mg, oral capsule dosage form. This prescription drug is labeled for twice-a-day dosing and distributed in a package of 100 capsules. The label includes storage instructions and manufacturer information for TWi Pharmaceuticals.*

FDA Label Image

Diltiazem HCl Extended-release Capsules, Usp 120 mg Bottle Label (Image 04)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP, 120 mg strength, manufactured by TWi Pharmaceuticals Inc. The label indicates a twice-a-day dosage, contains 100 capsules, and includes storage instructions and warnings to keep out of reach of children. It also displays the NDC 24979-183-01 and the lot and expiration date fields.*

* 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.