Diltiazem Hydrochloride
Product Images NDC 16714-555

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 16714-555). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Structure.jpg (Structure)

Chemical structure of Diltiazem Hydrochloride, showing its molecular arrangement including benzene rings, methoxy, acetoxy, sulfur, and hydrochloride components.*

FDA Label Image

Image-01 (Image 01)

Label for Diltiazem Hydrochloride Extended-Release Capsules 60 mg by Northstar Rx LLC. The label states the product contains 100 capsules, with instructions mentioning twice-a-day dosage. It includes storage conditions, manufacturer details, and a barcode, indicating it is a prescription medication (Rx only).*

FDA Label Image

Image-02 (Image 02)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP with a strength of 90 mg. The label specifies a twice-a-day dosage and a bottle containing 100 capsules. It is labeled as Rx only and manufactured for Northstar Rx LLC in Memphis, TN, with production by Glenmark Pharmaceuticals Limited in India. Storage instructions and other regulatory information are also included.*

FDA Label Image

Image-03 (Image 03)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, containing 100 capsules. The label shows storage instructions, dosage form as extended-release capsules, and manufacturer information including Northstar Rx LLC and Glenmark Pharmaceuticals Limited. The label also includes the NDC number 16714-555-01 and a barcode.*

* 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.