Diltiazem Hydrochloride Capsule, Coated, Extended Release
Product Images NDC 71335-0745

3 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 71335-0745). 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 (Dtz Image 1)

Chemical-structure (Dtz Image 1)
Chemical structure of diltiazem hydrochloride, illustrating the molecular arrangement of atoms and bonds including the benzene rings, sulfur, nitrogen, and hydrochloride (HCl) components.*
FDA Label Image

Lbl713350745

Lbl713350745
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, coated oral capsules. The label shows a package of 30 capsules produced by Bryant Ranch Prepack. It includes storage instructions, a barcode, and the manufacturer Par Pharmaceutical. The strength 120 mg is highlighted in a box.*
FDA Label Image

Lbl7133507452

Lbl7133507452
Label for Diltiazem HCL ER 120 mg capsule, extended-release coated oral dosage form. The label notes packaging by Bryant Ranch Prepack, Burbank, CA, and compares the product to Tiazac ER 120 mg capsule. It also includes storage instructions to keep at 20°-25°C (68°-77°F) and a caution to keep drugs out of reach of children. The package contains 30 capsules, and the NDC is 71335-0745-1.*

* 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.