Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 68682-367

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 68682-367). 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

This appears to be a label of a pharmaceutical product named "DILTIAZEM HYDROCHLORIDE Extended-Release Capsules, USP". It contains 90 capsules per pack and should not be used if the printed code is damaged. Other text on the label may not be readable as they contain non-English characters and may be errors.*

FDA Label Image

Image 02

FDA Label Image

Image 03

This is a product label for Diltiazem Hydrochloride extended-release capsules made by Bausch Health Companies in the US. Each capsule contains 240mg of the drug and the bottle contains 90 capsules. The National Drug Code (NDC) for this product is 68682-369-9405303. The other text appears to be unreadable and may not provide useful information.*

FDA Label Image

Image 04

This is a prescription medicine called Diltiazem Hydrochloride in 300mg extended-release capsules. It is manufactured by Bausch Health Companies Inc. in Canada. The description provides information about the quantity, warnings, and the manufacturer of the product.*

FDA Label Image

Image 05

This is a medication called Diltiazem Hydrochloride. It is an extended-release capsule and each capsule contains 360mg of the medication. It is manufactured by Bausch Health Companies and is not to be used if the bottle closure seal is broken. There are 90 capsules in the bottle.*

FDA Label Image

Image 06

This is a description for a medication called Diltiazem Hydrochloride. It is an extended-release capsule that contains 420mg of the drug. The usual dosage is once daily, and it is only available through prescription. It is manufactured by Bausch Health Companies in Canada and distributed by Oceanside Pharmaceutical in the United States. The bottle should not be used if the closure seal is broken. It should be stored at room temperature and kept out of reach of children. The full prescribing information can be found in the insert that comes with the medication.*

FDA Label Image

Chemical Structure (Tiazac 01)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.