Ondansetron Tablet, Film Coated
Product Images NDC 0904-6552

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 0904-6552). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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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This is a description of a unit dose package of Ondansetron tablets manufactured by Major Pharmaceuticals. Each film-coated tablet contains Ondansetron hydrochloride USP that is equivalent to ondansetron 8 mg. The dosage, administration, prescribing information, precautions, and warnings of the medication are available in the product insert. The medication should be stored at 20°-25°C and dispensed in a tight, light-resistant container. It is not child-resistant and is intended for institutional use only. The package also contains the distributor's information.*

FDA Label Image

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This is a description of Ondansetron tablets by Major Pharmaceuticals, containing 4mg of Ondansetron hydrochloride in each film-coated tablet. The dosage may vary as per the prescribed usage and other related information. The tablets are supplied in a pack of 100 tablets, stored at a controlled room temperature of 20°-25°C (68°-77°F), and must be kept in a tightly sealed, light-resistant container. This medication is not safe for children, as it is not child-resistant, and is intended only for institutional use. The output also contains information such as the manufacturer's address, NDC, and batch number.*

FDA Label Image

Structure (Structure)

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