Loratadine Tablet
Product Images NDC 62207-787

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Loratadine (NDC 62207-787). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Limited, 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

Loratadine-1000-bulk-jpg.jpg (Loratadine 1000 Bulk Jpg)

Loratadine Tablets USP, 10 mg label showing product name and strength, batch number placeholder, manufacturing and expiration date placeholders, manufacturing license number, NDC 62207-787-49, and storage instructions. The label indicates 1000 units in the package and states the product is for repacking only. Manufactured by Granules India Limited, located in Telangana, India.*

FDA Label Image

Loratidine-label-jpg (Loratidine Label Jpg)

Label for Loratadine Tablets USP 10 mg, each tablet containing 10 mg of Loratadine. The label includes batch number 7870001A, manufacture date 01/2020, expiration date 12/2022, and NDC number 62207-787-88. Manufactured by Granules India Limited, located in Telangana, India. Storage instructions specify 20°C to 25°C (68°F to 77°F). The package quantity is indicated as 5 x 20000 units.*

* 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.