Diltiazem Hydrochloride Extended-release Capsule, Extended Release
Product Images NDC 73190-013

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride Extended-release (NDC 73190-013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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

1 (011 01)

Packaging label for Diltiazem Hydrochloride Extended-Release Capsules USP 60 mg by AvKARE. The label indicates a 100 capsule count for oral administration with twice-a-day dosage. It includes storage instructions, active ingredient content per capsule, and cautions to keep medication out of reach of children.*

FDA Label Image

1 (012 01)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 90 mg, oral extended-release capsules. The label shows branding for AvKARE and indicates the product contains 100 capsules with a twice-a-day dosage. The label also lists storage instructions and manufacturer information for AvKARE, Pulaski, TN.*

FDA Label Image

1 (013 01)

Diltiazem Hydrochloride Extended-Release Capsules USP 120 mg by AvKARE. The label indicates a package of 100 capsules, prescription only, with directions for twice-a-day dosage. Storage instructions and warnings for use in pediatric patients are also included. The label displays the NDC number and a barcode.*

FDA Label Image

Chemical Structure (Diltiazem 01)

Chemical structure diagram of Diltiazem Hydrochloride, showing its molecular arrangement including aromatic rings, methoxy group, ester group, and hydrochloride component.*

* 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.