Levocetirizine Dihydrochloride Tablet
Product Images NDC 68071-3841

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Levocetirizine Dihydrochloride (NDC 68071-3841). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, 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

Pdp (68071 3841 9)

Label for Levocetirizine Dihydrochloride 5 mg tablets, a prescription oral tablet product by NuCare Pharmaceuticals, Inc. The label shows the product NDC 68071-3841-9, package size of 90 tablets, and storage instructions to keep out of reach of children and store at controlled temperature 68-77°F. Manufacturer address is Glenmark Pharmaceuticals Inc., USA.*

FDA Label Image

Y:\labeling\5 Us Labelling\2. Us Products_submissions\levocetirizine Dihydrochloride Tablets Usp, 5 mg\annual Reportable- Compendial Update Jun 2019\working Folder\spl\logo.jpg (Logo)

The image shows a white rectangular carton for LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg oral tablets. The packaging includes the brand name Genmark at the top, with distinctive red branding. The label indicates the product's active ingredient and strength, with a clean and simple design, but no additional details such as quantity or manufacturer beyond the Genmark logo are visible.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of levocetirizine dihydrochloride, showing its molecular components including chlorophenyl and piperazine groups with hydrochloride moieties.*

* 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.