Fexofenadine Hydrochloride Tablet, Film Coated
Product Images NDC 62207-889

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 Fexofenadine Hydrochloride (NDC 62207-889). 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

Fexofenadine-180mg-10s-carton (Fexofenadine 180mg 10s Carton)

Fexofenadine-180mg-10s-carton (Fexofenadine 180mg 10s Carton)
Packaging label for Fexofenadine HCl Tablets USP, 180 mg, film-coated oral tablets indicated for relief from hives. The carton contains 10 tablets and is labeled non-drowsy. The product is manufactured by Granules India Limited and distributed by Granules USA, Inc. The label includes a Drug Facts panel with detailed uses, warnings, directions, and inactive ingredients. The label features a barcode and is marked with the NDC 62207-891-51.*
FDA Label Image

Fexofenadine-180mg-10s-label (Fexofenadine 180mg 10s Label)

Fexofenadine-180mg-10s-label (Fexofenadine 180mg 10s Label)
Drug Facts label for Fexofenadine Hydrochloride 180 mg film-coated oral tablets by Granules India Limited. The label details the active ingredient, purpose as an antihistamine, usage instructions, warnings including severe allergy advice, precautions, directions for adults and children 12 and older, inactive ingredients, storage instructions, and contact information for questions or comments.*
FDA Label Image

Fexofenadine-180mg-blister-carton (Fexofenadine 180mg Blister Carton)

Fexofenadine-180mg-blister-carton (Fexofenadine 180mg Blister Carton)
Packaging label for Fexofenadine HCl Tablets USP 180 mg by Granules India Limited. The label shows a 70 count (7 x 10 tablets) film-coated oral tablet package for relief of hives and itching. The label includes a purple band highlighting 24-hour allergy relief, the NDC number 62207-891-58, and lists the tablet strength and form prominently on the front panel. Manufacturer and distributor information is on the side panel.*
FDA Label Image

Fexofenadine-60mg-10s-carton (Fexofenadine 60mg 10s Carton)

Fexofenadine-60mg-10s-carton (Fexofenadine 60mg 10s Carton)
Packaging label for Fexofenadine HCl Tablets, USP 60 mg, film-coated oral tablets by Granules India Limited. The label states the product is non-drowsy, used for hives relief, and contains 10 tablets per package. The label also includes detailed Drug Facts panels with active ingredient, uses, warnings, directions, and manufacturer information. Distributed by Granules USA, Inc.*
FDA Label Image

Fexofenadine-60mg-10s-label (Fexofenadine 60mg 10s Label)

Fexofenadine-60mg-10s-label (Fexofenadine 60mg 10s Label)
Drug Facts panel for Fexofenadine HCl Tablets USP 60 mg, an over-the-counter antihistamine used to reduce hives and relieve itching due to hives. The label provides active ingredient details, warnings including severe allergy and anaphylactic shock symptoms, usage instructions, contraindications, inactive ingredients, storage information, and a contact number for questions or comments. Manufactured by Granules India Limited and distributed by Granules USA, Inc.*
FDA Label Image

Fexofenadine-60mg-blister-carton (Fexofenadine 60mg Blister Carton)

Fexofenadine-60mg-blister-carton (Fexofenadine 60mg Blister Carton)
Fexofenadine Hydrochloride 60 mg film-coated tablets package label featuring the product as a non-drowsy antihistamine for reducing hives and relieving itching. The carton shows the NDC 62207-889-60, contains 72 tablets (8 x 9), and is labeled by Granules India Limited. The label includes a purple band noting comparison to Allegra Hives 12 Hour and various drug facts and directions on the unfolded sides.*

* 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.