Fexofenadine Hydrochloride Tablet
Product Images NDC 62207-765

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fexofenadine Hydrochloride (NDC 62207-765). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Ltd, 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.jpg (Fexofenadine 180mg 10s Carton)

Fexofenadine HCl Tablets, USP 180 mg is an oral antihistamine tablet for indoor/outdoor allergy relief, manufactured by Granules India Limited. The label states it is non-drowsy and comes in a package of 10 tablets. It includes drug facts with active ingredient, usage, warnings, directions, inactive ingredients, manufacturer and distributor information, and storage instructions.*

FDA Label Image

62207-765-51 (62207 765 51)

Label for Fexofenadine HCl Tablets, USP 60 mg by Granules India Ltd, an antihistamine for allergy relief. The label includes Drug Facts, usage, warnings, directions for different ages, and manufacturer information. The package contains 10 tablets with NDC 62207-765-51, made in India and distributed by Granules USA, Inc.*

FDA Label Image

62207-765-88 (62207 765 88)

Label for Fexofenadine Hydrochloride Tablets USP, 60 mg, film-coated oral tablets. Includes batch number, manufacturing and expiry dates placeholder, manufacturing license number, NDC number 62207-765-88, packaging quantity of 5 x 10,000 units, and storage instructions to protect from excessive moisture at 20°-25°C. Labeler is Granules India Ltd, with country of origin India noted.*

FDA Label Image

62207-766-35 (62207 766 35)

Label for Fexofenadine Hydrochloride Tablets USP, 180 mg, showing each film-coated tablet contains 180 mg of Fexofenadine Hydrochloride. The label includes batch details, manufacturing and expiration dates, manufacturing license number, NDC number 62207-766-35, storage instructions, caution for repacking, and barcodes. It specifies packaging as 5 units of 5000 tablets each and lists the country of origin as India.*

* 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.