Diltiazem Hydrochloride Tablet, Film Coated
Product Images NDC 0093-0319

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 0093-0319). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals 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

Structural Formula (Image 1)

Chemical structure of Diltiazem Hydrochloride showing its molecular arrangement, including benzene rings, methoxy and acetyl groups, and hydrochloride salt component.*

FDA Label Image

Label 30 mg, 100s (Image 2)

Label for Diltiazem Hydrochloride Tablets, USP 30 mg, film-coated oral tablets by Teva Pharmaceuticals USA, Inc. The label specifies 100 tablets per container, with instructions that tablets may be swallowed whole, crushed, or chewed but not split. Includes NDC 0093-0318-01 and a serialization coding area.*

FDA Label Image

Label 60 mg, 100s (Image 3)

Label for Diltiazem Hydrochloride Tablets USP 60 mg oral film-coated tablets, supplied in a bottle of 100 tablets by Teva Pharmaceuticals USA, Inc. The label includes dosage instructions note and storage information, with the NDC 0093-0319-01 and manufacturer details visible.*

FDA Label Image

Label 90 mg, 100 (Image 4)

Diltiazem Hydrochloride Tablets, USP 90 mg film-coated tablets label from Teva Pharmaceuticals USA, Inc. The package contains 100 tablets. The label displays NDC 0093-0320-01 and includes storage instructions and dispensing information. The dosage form is oral tablets, with a note that tablets may be swallowed whole, crushed, or chewed.*

FDA Label Image

Label 120 mg, 100 (Image 5)

Diltiazem Hydrochloride Tablets, USP 120 mg film-coated oral tablets in a 100-tablet package. The label includes directions stating tablets may be swallowed whole, crushed, or chewed. Manufactured by Teva Pharmaceuticals USA, Inc. The label features the product NDC 0093-0321-01 and storage instructions.*

* 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.