Cardizem La Tablet, Extended Release
Product Images NDC 0187-2050

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Cardizem La (NDC 0187-2050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch Health Us 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

Cardizem-la-image01 (Image 01)

Chemical structure of Diltiazem Hydrochloride, the active ingredient in Cardizem LA. The diagram shows the molecular arrangement of atoms including rings, functional groups, and substituents characteristic of this compound.*

FDA Label Image

Label 120mg

Label for Cardizem LA 120 mg extended-release tablets featuring the red and yellow color scheme with the product name and strength prominently displayed. The label indicates it contains 90 tablets, is Rx only, and is manufactured by Bausch Health US LLC. It includes a barcode, NDC number 0187-2045-90, and storage and warning information.*

FDA Label Image

Label 180mg

Label for Cardizem LA (Diltiazem Hydrochloride) 180 mg extended-release oral tablets, a prescription drug. The label shows a package size of 90 tablets and highlights the strength as 180 mg. It features the Bausch Health logo and includes manufacturer information for Bausch Health US, LLC and Bausch Health Companies Inc., Canada. The NDC code 0187-2046-90 is displayed prominently at the top.*

FDA Label Image

Label 240mg

Label for Cardizem LA 240 mg extended-release tablets by Bausch Health US LLC. The label features a yellow background with red and black text, stating the active ingredient Diltiazem Hydrochloride and quantity of 90 tablets. It includes storage instructions, warnings, and manufacturer information, with barcode and NDC 0187-2047-90.*

FDA Label Image

Label 300mg

Label for Cardizem LA 300 mg extended-release oral tablets by Bausch Health US LLC. The front displays the proprietary name with strength on a yellow background, indicating a package of 90 tablets. Additional text includes storage instructions, manufacturer details, and barcode.*

FDA Label Image

Label 360mg

Label for Cardizem LA 360 mg extended-release oral tablets by Bausch Health US LLC. The label shows the product name with the active ingredient Diltiazem Hydrochloride, package quantity of 90 tablets, and storage instructions. It includes an NDC number, barcode, and manufacturing info with the product of Canada statement.*

FDA Label Image

Label 420mg

Packaging label for Cardizem LA 420 mg extended-release tablets containing Diltiazem Hydrochloride. The label shows the product name, strength, dosage form, and a count of 90 tablets. It includes manufacturer information for Bausch Health US LLC and storage instructions. The label also features a barcode and the NDC 0187-2050-90.*

* 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.