Ondansetron
Product Images NDC 67296-0847

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 67296-0847). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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 showing the arrangement of atoms including an indole ring, a ketone group, and an imidazole ring with associated hydrochloride and water molecules.*

FDA Label Image

Showbox4mg (Showbox4mg)

Ondansetron Hydrochloride Tablets 4 mg unit dose packaging label. The label shows a quantity of 100 unit dose tablets arranged in 10 blister cards of 10 tablets each. The label mentions Rx only and includes the logo of Sun Pharma. The NDC on the label is 62756-130-02.*

FDA Label Image

Showbox8mg (Showbox8mg)

Packaging label for Ondansetron Hydrochloride Tablets 8 mg, labeled as unit dose with a quantity of 100 tablets (10x10). The label includes the NDC 62756-131-02 and the Sun Pharma logo. The labeler shown is Sun Pharma.*

FDA Label Image

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

Chemical structure of ondansetron showing its molecular arrangement with carbon, nitrogen, oxygen atoms and bond connections, including characteristic ring systems and functional groups.*

FDA Label Image

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

Ondansetron Hydrochloride Tablets 4 mg label showing a bottle containing 30 tablets. Product marked Rx only, distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharmaceutical Industries Ltd., India. The label includes storage instructions and dosage information disclaimers.*

FDA Label Image

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

Ondansetron Hydrochloride Tablets 8 mg label from RedPharm Drug showing a 30-tablet prescription package. The label includes storage instructions and manufacturer details for Sun Pharmaceutical Industries Ltd. The NDC 62756-131-01 is printed above the product name along with the Sun Pharma logo.*

FDA Label Image

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

Ondansetron Orally Disintegrating Tablets, USP 4 mg packaging label showing a 30 tablet count (3 blister cards each with 10 tablets). The label includes the NDC 62756-240-64 and indicates it is manufactured by Sun Pharmaceutical Industries Ltd and distributed by Sun Pharmaceutical Industries, Inc. Storage instructions and warnings for phenylketonurics are also visible.*

FDA Label Image

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

Ondansetron Orally Disintegrating Tablets USP 8 mg packaging label displaying the product name, strength, dosage form, and quantity of 30 tablets in 3 blister cards of 10 each. The label also includes manufacturer Sun Pharmaceutical Industries Ltd. with location in Gujarat, India, and distributor Sun Pharmaceutical Industries, Inc. in Cranbury, NJ. Storage instructions and warnings are printed, as well as a barcode and Sun Pharma logo.*

FDA Label Image

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

Ondansetron Orally Disintegrating Tablets, USP 4 mg label showing a 30-tablet package. Manufactured by Sun Pharmaceutical Industries Ltd., and distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ. The label includes NDC 62756-240-83, dosage storage instructions, phenylalanine warning, and a barcode.*

FDA Label Image

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

Ondansetron Orally Disintegrating Tablets, USP 8 mg tablet label by RedPharm Drug. The label states 30 tablets, Rx only, and includes storage instructions at 20° to 25°C. Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ and manufactured by Sun Pharmaceutical Industries Ltd., Gujarat, India. It warns phenylketonurics to note phenylalanine content.*

* 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.