Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 62756-131

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 62756-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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 (Chemical Structure)

Chemical structure of Ondansetron hydrochloride dihydrate as depicted in the image, showing its molecular framework including benzene and imidazole rings with associated functional groups.*

FDA Label Image

Showbox4mg (Showbox4mg)

Packaging label for Ondansetron Hydrochloride Tablets 4 mg by Sun Pharmaceutical Industries Limited. The label shows the drug strength as 4 mg and the packaging as 100 unit dose tablets (10x10). It includes the NDC number 62756-130-02 and the Sun Pharma logo.*

FDA Label Image

Showbox8mg (Showbox8mg)

Ondansetron Hydrochloride Tablets 8 mg unit dose packaging label showing a quantity of 100 tablets (10x10 unit dose). The label displays the NDC number 62756-131-02 and the Sun Pharmaceutical Industries Limited logo.*

FDA Label Image

Spl-ondansetron-chemical-structure (Spl Ondansetron Chemical Structure)

Chemical structure diagram of ondansetron, showing its molecular framework including a carbazole group connected to a methyl-substituted imidazole.*

FDA Label Image

Spl-ondansetron-hcl-label-4mg (Spl Ondansetron HCl Label 4mg)

ONDANSETRON Hydrochloride Tablets 4 mg label for a 30-tablet package. The label states each film-coated tablet contains 5 mg of ondansetron hydrochloride USP dihydrate, equivalent to 4 mg ondansetron. Manufactured by Sun Pharmaceutical Industries Ltd., India, and distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ. Storage instructions and dosage note included.*

FDA Label Image

Spl-ondansetron-hcl-label-8mg (Spl Ondansetron HCl Label 8mg)

Label for Ondansetron Hydrochloride Tablets 8 mg by Sun Pharmaceutical Industries Limited. The label indicates a 30-tablet package supplied by Sun Pharmaceutical Industries, with storage instructions and manufacturer details from Gujarat, India. It includes an NDC barcode and dosage note referencing the package insert.*

FDA Label Image

Spl-ondansetron-odt-4mg-showbox (Spl Ondansetron Odt 4mg Showbox)

Ondansetron Orally Disintegrating Tablets 4 mg carton label showing Rx only status, 30 tablets total in 3 blister cards with 10 tablets each. Label includes the NDC 62756-240-64 and the Sun Pharmaceutical Industries Limited logo.*

FDA Label Image

Spl-ondansetron-odt-8mg-showbox (Spl Ondansetron Odt 8mg Showbox)

Ondansetron Orally Disintegrating Tablets 8 mg packaging label showing the product name and strength prominently. The label states the package contains 30 tablets, arranged as 3 blister cards each with 10 tablets. It includes 'Rx only' and the Sun Pharmaceutical Industries Limited logo.*

FDA Label Image

Spl-ondansetron-odt-label-4mg (Spl Ondansetron Odt Label 4mg)

Ondansetron Orally Disintegrating Tablets 4 mg label from Sun Pharmaceutical Industries Limited. The label states each tablet contains 4 mg ondansetron USP, with 30 tablets in the package. It includes storage instructions, a phenylketonurics warning, manufacturer and distributor information, and a barcode.*

FDA Label Image

Spl-ondansetron-odt-label-8mg (Spl Ondansetron Odt Label 8mg)

Ondansetron Orally Disintegrating Tablets 8 mg label from Sun Pharmaceutical Industries Limited. The label includes dosage strength (8 mg), quantity (30 tablets), and indicates that each tablet contains 8 mg ondansetron USP. It advises storage at 20° to 25°C, mentions phenylalanine content, and states approximate disintegration time of 60 seconds. Manufacturer and distributor details in India and the U.S. are also shown.*

* 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.