Loratadine Tablet
Product Images NDC 68084-248

3 FDA label images from American Health Packaging · 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 Loratadine (NDC 68084-248). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

10 mg Loratadine Tablet Blister (10 mg Loratadine Tablet Blister)

10 mg Loratadine Tablet Blister (10 mg Loratadine Tablet Blister)
This image shows multiple identical labels for Loratadine 10 mg oral tablets by American Health Packaging. Each label includes the proprietary and generic name Loratadine, strength 10 mg, dosage form tablet, barcode, lot number, expiration date, and the labeler's location in Columbus, Ohio.*
FDA Label Image

10 mg Loratadine Tablets Carton (10 mg Loratadine Tablets Carton)

10 mg Loratadine Tablets Carton (10 mg Loratadine Tablets Carton)
Loratadine Tablets USP 10 mg oral tablets by American Health Packaging. The package contains 100 tablets in 10 blister packs of 10 each. The label highlights the non-drowsy 24-hour allergy relief indication for indoor and outdoor allergies. Drug Facts information includes active ingredient Loratadine 10 mg per tablet, uses, warnings, directions, and storage details.*
FDA Label Image

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Loratadine 10 mg white round tablet with an imprint that appears to read 'R 52 5'. The tablet is shown from both front and back sides on a gray scale background with a millimeter measurement ruler along the left and bottom edges.*

* 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.