Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 68682-372

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 68682-372). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oceanside Pharmaceuticals, 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

Image 01

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg by Oceanside Pharmaceuticals. The label indicates a 90-capsule bottle with a warning not to use if the bottle closure seal is broken. The label shows the NDC code and directions for storage and dispensing.*

FDA Label Image

Image 02

Label for Diltiazem Hydrochloride Extended Release Capsules, 180 mg strength from Oceanside Pharmaceuticals. The label indicates 90 capsules and includes details such as a barcode, NDC (68682-368-90), and usage instructions including storage and handling. It is marked Rx only.*

FDA Label Image

Image 03

Label for Diltiazem Hydrochloride 240 mg extended-release capsules, USP, distributed by Oceanside Pharmaceuticals. The label indicates a package containing 90 capsules and includes storage instructions and safety warnings. The label also shows the NDC 68682-369-90 and notes Rx only status.*

FDA Label Image

Image 04

Label for Diltiazem Hydrochloride Extended-Release Capsules 300 mg by Oceanside Pharmaceuticals. The label states 90 capsules, includes an NDC code (68682-370-90), and mentions drug release testing and storage conditions. The packaging is primarily light blue and white with the product name prominently displayed.*

FDA Label Image

Image 05

Label for Diltiazem Hydrochloride Extended-Release Capsules USP, 360 mg strength. The label shows the dosage form as extended-release capsules, contains 90 capsules per container, and indicates the product is distributed by Oceanside Pharmaceuticals. It includes storage instructions and a barcode, along with the NDC number 68682-371-90 and a clear statement that it is Rx only.*

FDA Label Image

Image 06

Label for Diltiazem Hydrochloride Extended Release Capsules, USP containing 420 mg per capsule. The package holds 90 capsules and is distributed by Oceanside Pharmaceuticals, a division of Bausch Health US, LLC. Manufactured by Bausch Health Companies Inc. in Canada. The label includes dosage and storage instructions, an NDC number 68682-372-90, and a barcode.*

FDA Label Image

Chemical Structure (Tiazac 01)

Chemical structure diagram of diltiazem hydrochloride, showing its molecular components including aromatic rings, sulfur, oxygen, nitrogen, and associated functional groups, along with its hydrochloride form indicated.*

* 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.