Diltiazem Hydrochloride Tablet, Extended Release
Product Images NDC 68682-708

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 68682-708). 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

A Molecule Of A Chemical Formulaai-generated Content May Be Incorrect. (Image 01)

Chemical structure of diltiazem hydrochloride showing molecular bonds and functional groups including methoxy, acetoxy, and amine groups consistent with the active ingredient diltiazem hydrochloride.*

FDA Label Image

120 mg Carton (Label 120mg)

Label for Diltiazem Hydrochloride Extended-Release Tablets 120 mg, oral dosage form, supplied by Oceanside Pharmaceuticals. The label shows a 90-tablet package, the NDC code 68682-704-90, and storage warnings. The label also includes distributor and manufacturer information: distributed by Oceanside Pharmaceuticals, a division of Bausch Health US, LLC, Bridgewater, NJ, and manufactured by Bausch Health Companies Inc., Steinbach, Canada. The design features a blue and white color scheme with the Oceanside Pharmaceuticals logo.*

FDA Label Image

180 mg Carton (Label 180mg)

Label for Diltiazem Hydrochloride Extended-Release Tablets 180 mg by Oceanside Pharmaceuticals. The label includes the NDC 68682-705-90, indicates prescription use only, and features a barcode. The label states 90 tablets per container, with storage instructions and manufacturer details for Bausch Health Companies Inc., Canada.*

FDA Label Image

240 mg Carton (Label 240mg)

Label for Diltiazem Hydrochloride Extended-Release Tablets 240 mg oral tablets from Oceanside Pharmaceuticals. The label shows the NDC 68682-706-90, quantity of 90 tablets, and includes storage and handling information, distribution by Oceanside Pharmaceuticals, and manufacturing by Bausch Health Companies Inc. in Canada.*

FDA Label Image

300 mg Carton (Label 300mg)

Label for Diltiazem Hydrochloride Extended-Release Tablets 300 mg oral tablets, supplied in a package of 90 tablets. The label shows the NDC 68682-707-90 and states prescription use only. It is distributed by Oceanside Pharmaceuticals and manufactured by Bausch Health Companies Inc. in Canada. Storage instructions and warnings are also included on the label.*

FDA Label Image

360 mg Carton (360mg Label)

Label for Diltiazem Hydrochloride Extended-Release Tablets 360 mg by Oceanside Pharmaceuticals. The label indicates 90 tablets per container. It includes storage instructions, warnings, and manufacturer details, with a barcode and NDC number 68682-708-90. The design features a blue and purple color scheme with the Oceanside Pharmaceuticals logo.*

FDA Label Image

420 mg Carton (Label 420mg)

Label for Diltiazem Hydrochloride Extended-Release Tablets 420 mg by Oceanside Pharmaceuticals. The label shows the product name prominently with a blue bar displaying the 420 mg strength. It indicates the package contains 90 tablets. The label includes NDC 68682-709-90, storage instructions, warnings to keep out of reach of children, and distributor and manufacturer information. The label design features a barcode and Oceanside Pharmaceuticals logo.*

* 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.