Diltiazem Hydrochloride
Product Images NDC 33261-847

3 FDA label images from Aidarex Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 33261-847). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals Llc, 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

De202a27-figure-01 (Diltiazem HCl Er 180mg Cap For Actavis 1)

De202a27-figure-01 (Diltiazem HCl Er 180mg Cap For Actavis 1)
Chemical structure of diltiazem hydrochloride showing its molecular composition with labeled functional groups, including methoxy, ester, and amine groups, along with its hydrochloride salt form.*
FDA Label Image

De202a27-figure-03 (Diltiazem HCl Er 180mg Cap For Actavis 2)

De202a27-figure-03 (Diltiazem HCl Er 180mg Cap For Actavis 2)
Diltiazem Hydrochloride 180 mg extended-release capsules bottle label by Aidarex Pharmaceuticals LLC. The label shows the product name, strength, dosage form as capsules, and the quantity as 100 capsules per bottle. The label includes details such as the NDC 33261-847 and a barcode.*
FDA Label Image

Image Label (Diltiazem HCl Er 180mg Cap For Actavis 3)

Image Label (Diltiazem HCl Er 180mg Cap For Actavis 3)
Label for Diltiazem ER 180 mg extended-release capsules, 30 count, distributed by Aidarex Pharmaceuticals LLC. The label shows the active ingredient as diltiazem hydrochloride 180 mg per capsule. The product is generic for Cardizem-CD, manufactured by Actavis Elizabeth LLC in Elizabeth, New Jersey. The label includes NDC number 33261-0847-30 and dosage instructions placeholders.*

* 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.