Diltiazem Hydrochloride Extended-release
Product Images NDC 42291-029

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 Extended-release (NDC 42291-029). 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

100 (028 01)

100 (028 01)
Label for Diltiazem Hydrochloride Extended-Release Capsules USP, 60 mg strength, by AvKARE. The label indicates a twice-a-day dosage with 100 capsules per container. It includes storage conditions and warnings such as keeping the container tightly closed and out of reach of children.*
FDA Label Image

100 (029 01)

100 (029 01)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP, 90 mg strength, containing 100 capsules. The label indicates a twice-a-day dosage and includes the NDC 42291-029-01. It is labeled Rx only and manufactured by AvKARE.*
FDA Label Image

100 (030 01)

100 (030 01)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg by AvKARE. The label indicates twice-a-day dosage, contains 100 capsules, and includes storage instructions and warnings. It also displays the NDC number 42291-030-01, barcodes, and manufacturer information.*
FDA Label Image

Chemical Structure (Diltiazem 01)

Chemical Structure (Diltiazem 01)
Chemical structure of Diltiazem Hydrochloride, showing its molecular framework including benzene rings, sulfur atom, and functional groups such as methoxy (OCH3), ester (OOCCH3), and amide linkages.*

* 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.