Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 68788-7870

4 FDA label images from Preferred Pharmaceuticals Inc. · 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 68788-7870). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred 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.

Product Images & Figures Index

FDA Label Image

Image (Image 01)

Image (Image 01)
Chemical structure of diltiazem hydrochloride, showing molecular bonds and groups including methoxy, acetyl, and tertiary amine functional groups.*
FDA Label Image

Image (Image 02)

Image (Image 02)
A data table presenting adverse reactions during placebo-controlled angina and hypertension trials comparing diltiazem hydrochloride extended-release capsules (n=607) with placebo (n=301). It lists adverse reactions such as headache, dizziness, bradycardia, AV block first degree, edema, and asthenia, with corresponding incidence percentages for each group.*
FDA Label Image

Image (Image 04)

Image (Image 04)
FDA Label Image

Diltazem Hydrochloride Extended-release Cap Usp 120mg (Image 05)

Diltazem Hydrochloride Extended-release Cap Usp 120mg (Image 05)
Label for diltiazem hydrochloride extended-release capsules USP 120 mg by Preferred Pharmaceuticals Inc. The label indicates the product as a generic to Dilt XR, with dosage form extended-release capsule. It includes directions for use in English and Spanish, storage instructions, and manufacturing details from Ingenus Pharmaceuticals, LLC. The capsule is described as white and imprinted with N365 120.*

* 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.