Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 0378-6090

View Photos of 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 Diltiazem Hydrochloride (NDC 0378-6090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals Inc., 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

Image 01

Image 01
Chemical structure diagram of diltiazem hydrochloride, showing the arrangement of aromatic rings, sulfur, oxygen, nitrogen atoms, and associated side groups, including the hydrochloride component.*
FDA Label Image

Image 02

Image 02
Label for Diltiazem Hydrochloride 60 mg Extended-Release oral capsules by Mylan Pharmaceuticals Inc. The label indicates twice-a-day dosage and contains 100 capsules. It includes dosage strength, administration instructions, storage directions, and the Mylan logo.*
FDA Label Image

Image 03

Image 03
Diltiazem HCl Extended-Release Capsules, USP, 90 mg strength by Mylan Pharmaceuticals Inc. The label indicates twice-a-day dosage with 100 capsules per bottle. It notes the active ingredient diltiazem hydrochloride equivalent to 82.7 mg diltiazem, cautions for storage, and child-resistant packaging.*
FDA Label Image

Image 04

Image 04
Label for Diltiazem Hydrochloride extended-release capsules, USP 120 mg, by Mylan Pharmaceuticals Inc. The label states 'Twice-a-Day Dosage' and includes the NDC 0378-6120-01. Packaging contains 100 capsules, with instructions for storage and dispensing in a tight, child-resistant container. The label indicates it is Rx only and provides lot and expiration space.*

* 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.