Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 71335-0867

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 (NDC 71335-0867). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemical Structure (Diltiazem 01)

FDA Label Image

Label Image (Lbl713350634)

Label Image (Lbl713350634)
Diltiazem ER 180 mg Capsule packaging label from Bryant Ranch Prepack. The label indicates an extended-release capsule with a comparison to Tiazac 180 mg Capsule by Valeant Pharmaceuticals International. The package contains 30 capsules and includes storage instructions at room temperature 20-25°C (68-77°F). The label features a barcode and the NDC number 7133506341, alongside a description of capsule color as dark green opaque/light green opaque.*
FDA Label Image

Label Image (Lbl713350867)

Label Image (Lbl713350867)
Label for Diltiazem Hcl ER 240mg Capsule, extended release oral capsules packaged by Bryant Ranch Prepack in Burbank, CA. The label compares this product to Cardizem 240mg Capsule, lists storage at 20°-25°C, and includes a barcode and NDC 7133508671. The package quantity is 30 capsules.*
FDA Label Image

Label Image (Lbl713351389)

Label Image (Lbl713351389)
Label for Cartia XT 120 mg extended release capsule, packaged by Bryant Ranch Prepack in Burbank, CA. The label indicates a light green opaque capsule, bottle quantity 120, with storage instructions at 20°-25°C (68°-77°F), and a barcode with NDC 71335-1389-1. The package size is 30 capsules.*

* 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.