Loratadine 10mg Tablet
Product Images NDC 25000-092

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Loratadine 10mg (NDC 25000-092). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marksans Pharma 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-tablets-14ct-blister-carton (Loratadine Tablets 14ct Blister Carton)

Loratadine-tablets-14ct-blister-carton (Loratadine Tablets 14ct Blister Carton)
The image shows the flattened packaging label for Loratadine Tablets USP, 10 mg by Marksans Pharma Limited. The carton highlights 14 tablets with 24-hour non-drowsy antihistamine relief for indoor and outdoor allergies. The box includes drug facts, directions, warnings, inactive ingredients, and contact information. The label also states it is tamper-evident and not child-resistant.*
FDA Label Image

Loratadine-tablets-150ct-carton (Loratadine Tablets 150ct Carton)

Loratadine-tablets-150ct-carton (Loratadine Tablets 150ct Carton)
Packaging label for Loratadine 10mg tablets, an oral antihistamine by Marksans Pharma Limited. The label highlights the product's 10 mg strength, tablet form, and 150 count. Included are drug facts, warnings, directions, inactive ingredients, manufacturer details, and a barcode. The label also states that the product is made in India and compares to Claritin tablets.*
FDA Label Image

Loratadine-tablets-150ct-label (Loratadine Tablets 150ct Label)

Loratadine-tablets-150ct-label (Loratadine Tablets 150ct Label)
Drug Facts text panel for Loratadine 10 mg tablets by Marksans Pharma Limited includes sections on active ingredient, uses, warnings, directions, other information, inactive ingredients, and questions or comments. It provides typical dosage instructions and safety warnings for adults, children, pregnant or breastfeeding women, and storage instructions.*
FDA Label Image

Loratadine-tablets-30-ct-label (Loratadine Tablets 30 Ct Label)

Loratadine-tablets-30-ct-label (Loratadine Tablets 30 Ct Label)
Drug Facts text panel for Loratadine 10mg tablets by Marksans Pharma Limited includes active ingredient, uses such as relief from indoor and outdoor allergy symptoms, warnings including allergic reactions and kidney or liver disease, directions for adults and children, inactive ingredients, tamper-evident information, and a contact number for questions or comments.*
FDA Label Image

Loratadine-tablets-30ct-carton (Loratadine Tablets 30ct Carton)

Loratadine-tablets-30ct-carton (Loratadine Tablets 30ct Carton)
Packaging label for Loratadine 10 mg tablets by Marksans Pharma Limited. The label includes Drug Facts with active ingredient, uses, warnings, directions, inactive ingredients, and contact information. The front panel highlights Loratadine USP 10 mg, an antihistamine for allergy relief, and specifies a 30-tablet count. The label also contains barcodes and manufacturing details.*
FDA Label Image

Loratadine-tablets-365ct-label (Loratadine Tablets 365ct Label)

Loratadine-tablets-365ct-label (Loratadine Tablets 365ct Label)
Drug Facts panel for Loratadine 10 mg tablets by Marksans Pharma Limited. The panel includes purpose, uses, warnings, directions, inactive ingredients, and tamper-evidence information. The label indicates the tablets relieve allergy symptoms and specifies dosage directions for adults and children over 6 years. It notes storage conditions and FDA dissolution test standards.*

* 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.