Diltiazem Hydrochloride Tablet, Extended Release
Product Images NDC 69097-995

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 69097-995). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cipla Usa, Inc., 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

120mg_90.jpg (120mg 90)

Label for Diltiazem Hydrochloride Extended-Release Tablets, 120 mg strength. The label shows the product name, strength, dosage form, quantity of 90 tablets, and labeler Cipla USA, Inc. It includes usage instructions, storage conditions, and cautions, with a barcode and NDC number 69097-992-05.*

FDA Label Image

180_30.jpg (180 30)

Label for Diltiazem Hydrochloride Extended-Release Tablets 180 mg, oral tablets, packaged in a 30-count container. The label indicates the product is manufactured for Cipla USA, Inc. It includes dosage strength, quantity, and manufacturer information along with a barcode and storage instructions.*

FDA Label Image

Image Description (180 90)

Label for Diltiazem Hydrochloride Extended-Release Tablets shows a strength of 180 mg. The package contains 90 tablets. The label identifies Cipla USA, Inc. as the manufacturer and includes standard storage and handling instructions along with the dosage form as extended-release tablets for oral use.*

FDA Label Image

240_30.jpg (240 30)

DILTIAZEM HYDROCHLORIDE extended-release tablets 240 mg in an oral dosage form. The label indicates a package size of 30 tablets and is labeled by Cipla USA, Inc. It includes standard storage and dosing instructions, along with barcode and regulatory information.*

FDA Label Image

240_90.jpg (240 90)

Label for Diltiazem Hydrochloride Extended-Release Tablets, 240 mg, oral dosage form. The package contains 90 tablets. The label shows storage instructions, the labeler Cipla USA, Inc., and mentions manufacturing by SciGen Pharmaceuticals, Inc. It includes a barcode and usage warnings such as 'Rx Only' and keeping out of reach of children.*

FDA Label Image

300_30.jpg (300 30)

Label for Diltiazem Hydrochloride Extended-Release Tablets, 300 mg, by Cipla USA, Inc. The label indicates an oral extended-release tablet with a package containing 30 tablets. It includes dosage and storage information and a barcode on the right side.*

FDA Label Image

300mg_90.jpg (300 90)

Label for Diltiazem Hydrochloride Extended-Release Tablets 300 mg by Cipla USA, Inc. The label indicates the oral tablet form, package count of 90 tablets, and includes storage instructions as well as manufacturer details. The NDC 69097-995-05 is visible.*

FDA Label Image

360mg-30s.jpg (360 30)

Diltiazem Hydrochloride Extended-Release Tablets 360 mg in oral tablet form, packaged in a box containing 30 tablets. The label states the product is manufactured by Cipla USA, Inc. and includes warnings and storage instructions. The label features the Cipla logo and a barcode.*

FDA Label Image

360_90.jpg (360 90)

Diltiazem Hydrochloride Extended-Release Tablets 360 mg in a 90-tablet bottle. The label displays dosage strength, quantity, and manufacturer Cipla USA, Inc., with usage instructions and warnings on the side panel. The label includes a barcode and lot information.*

FDA Label Image

420_30.jpg (420 30)

Diltiazem Hydrochloride Extended-Release Tablets 420 mg oral tablets. The blue and white carton contains 30 tablets. The label includes dosage information and manufacturing details, showing Cipla USA, Inc. as the labeler.*

FDA Label Image

420_90.jpg (420 90)

The label for Diltiazem Hydrochloride Extended-Release Tablets 420 mg shows the product name, strength, and dosage form. It is an oral tablet with 90 tablets per container. The labeler is Cipla USA, Inc. Instructions include storage conditions and handling, with the label designed for prescription use only.*

FDA Label Image

Diltiazem_120mg 30.jpg (Diltiazem 120mg 30)

The packaging label for Diltiazem Hydrochloride Extended-Release Tablets displays the 120 mg strength. The label indicates 30 tablets per container, oral route, and includes the Cipla USA, Inc. labeler name. It also lists storage instructions and an NDC number 69097-992-02.*

FDA Label Image

Structure.jpg (Structure)

Chemical structure of diltiazem hydrochloride, showing its molecular framework with rings, functional groups, and the hydrochloride component.*

* 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.