Granisetron Hydrochloride
Product Images NDC 17478-546

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 17478-546). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, 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

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Chemical structure of Granisetron Hydrochloride, depicting its molecular arrangement including a bicyclic ring system, a methyl group attached to nitrogen atoms, and associated hydrochloride (HCl).*
FDA Label Image

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Granisetron Hydrochloride Injection USP 1 mg/mL single-dose vial label showing usage instructions for intravenous administration. The label includes storage conditions (20° to 25°C), protection from light, and manufacturer Akorn, Inc. It also features the NDC number 17478-546-02 and areas for lot and expiration dates.*
FDA Label Image

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Label for Granisetron Hydrochloride Injection USP 1 mg/mL single-dose vial by Akorn. The label specifies intravenous use only, provides dosage and storage instructions, and lists ingredients including granisetron hydrochloride and preservatives. The NDC is 17478-546-02. The label includes warnings to avoid freezing and protect from light.*
FDA Label Image

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Granisetron Hydrochloride Injection, USP 4 mg/4 mL (1 mg/mL) multi-dose vial label. The label states it is for intravenous use only and includes storage instructions to keep at 20° to 25°C (68° to 77°F), avoid freezing, and protect from light. It is manufactured by Akorn, Inc.*
FDA Label Image

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Label for Granisetron Hydrochloride Injection, USP 4 mg/4 mL (1 mg/mL) by Akorn. The label indicates a 4 mL multi-dose vial for intravenous use only. It includes dosage, storage instructions, active and inactive ingredients, preservation information, and manufacturer details at Lake Forest, IL.*

* 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.