Desloratadine Tablet, Film Coated
Product Images NDC 68180-153

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Desloratadine (NDC 68180-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

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Chemical structure of desloratadine, depicting the molecular framework including chlorine, nitrogen atoms, and ring formations consistent with its antihistamine composition.*

FDA Label Image

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Desloratadine Tablet USP 5 mg film-coated tablet labels printed for Lupin Pharmaceuticals, Inc. Each label shows the product name, strength (5 mg), designation as Rx only, manufacturer Lupin Pharmaceuticals, Inc., along with NDC code 68180-153-11, barcodes, and spaces for lot number and expiration date. The labels are arranged in a sheet format for dispensing or packaging use.*

FDA Label Image

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Label for Desloratadine Tablets USP 5 mg, oral film-coated tablets by Lupin Pharmaceuticals, Inc. The label indicates a package size of 100 tablets, includes the NDC 68180-153-01, barcode, storage instructions, and manufacturer information for Lupin Pharmaceuticals and Lupin Limited, India.*

FDA Label Image

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Packaging label for Desloratadine Tablets USP 5 mg by Lupin Pharmaceuticals, Inc. The label indicates film-coated tablets with 30 unit dose tablets (3 strips of 10 tablets). It includes storage instructions, pharmacist dispensing information, and manufacturer details for Lupin Limited, India. The NDC number 68180-153-12 is shown with a barcode on the bottom panel.*

* 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.