Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 60505-0015

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 60505-0015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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

120mg-100btl (120mg 100btl)

Label for DILT-XR 120 mg extended-release capsules containing diltiazem hydrochloride. The label states the dosage form as extended-release capsules with once-a-day dosage, listing 100 capsules per bottle. It includes storage instructions and manufacturer details for Apotex Corp., Toronto, Ontario, Canada, and Weston, Florida. The label features the NDC 60505-0014-6 and a barcode.*

FDA Label Image

180mg-100btl (180mg 100btl)

Label for DILT-XR Diltiazem Hydrochloride Extended-Release Capsules, USP 180 mg, showing a 100 capsule package. The label includes storage instructions, manufacturing details by Apotex Inc., and states the dosage form as extended-release capsules to be taken once daily. The labeler is Apotex Corp.*

FDA Label Image

240mg-100btl (240mg 100btl)

Label for DILT-XR Diltiazem Hydrochloride Extended-Release Capsules, USP 240 mg, oral capsule, once-a-day dosage. Package contains 100 capsules. Manufactured and labeled by Apotex Corp. Storage instructions and handling cautions are printed on the label along with the NDC 60505-0016-6 and a barcode.*

FDA Label Image

Structure (Structure)

Chemical structure of diltiazem hydrochloride, showing its molecular framework including benzene rings and functional groups, along with the 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.