Granisetron Hydrochloride Tablet
Product Images NDC 51991-735

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Granisetron Hydrochloride (NDC 51991-735). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Breckenridge Pharmaceutical, Inc., 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

Chemical Structure (Granisetron 01)

FDA Label Image

Principal Display Panel (2 Tablet Blister Pack Carton)

Principal Display Panel (2 Tablet Blister Pack Carton)
Each tablet of Granisetron Hydrochloride contains 1.12 mg of granisetron hydrochloride USP equivalent to granisetron, 1 mg. It is a medication used to prevent nausea and vomiting caused by cancer chemotherapy and radiation therapy. The suggested dosage is 2 mg once daily or 1 mg twice daily. For chemotherapy administration, two tablets of 1 mg each are taken up to 1 hour before chemotherapy in the 2mg once daily regimen. In the 1 mg twice daily regimen, the first 1 mg tablet is given 1 hour before chemotherapy, and the second one 12 hours after the first. Two 1mg tablets of Granisetron are taken within 1 hour of radiation for radiation therapy. This drug should be stored between 20°C to 26°C, protected from light, and kept in its carton until the time of use. The manufacturing details and dosage information can be found in the accompanying prescribing information.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.