Granisetron Hydrochloride Tablet, Film Coated
Product Images NDC 63850-0005

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Granisetron Hydrochloride (NDC 63850-0005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natco 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

Granisetron Hydrochloride 1 mg _blister Of 2x20's (Grani.fig2)

FDA Label Image

Granisetron Hydrochloride 1 mg _ Carton 2x20's (Grani.fig3)

FDA Label Image

Granisetron Hydrochloride 1 mg_ Foil Of 2 Tablets (Grani.fig4)

Granisetron Hydrochloride 1 mg_ Foil Of 2 Tablets (Grani.fig4)
This is a description of a pharmaceutical product, Granisetron Hydrochloride, in the form of a tablet with 1mg dosage. The product has a National Drug Code (NDC) 63850-0005-2 and is manufactured by Natco Pharma Limited located in Kothur-509 228, Andhra Pradesh, India. Other details such as LOT and expiration date are not available in the text.*
FDA Label Image

Granisetron Hydrochloride1mg-carton 2 Tablets (Granifig5)

Granisetron Hydrochloride1mg-carton 2 Tablets (Granifig5)
This appears to be the description of a medication called Granisetron Hydrochloride Tablets USP, 1 mg. It includes details about the dosage and ingredients found in each tablet. The tablet is not child-resistant, and its packaging does not provide any protective features. The text also includes NDC numbers to help identify the medication.*
FDA Label Image

Granisetron Hydrochloride Structure (Granisetron Structure)

* 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.