Ondansetron Tablet, Film Coated
Product Images NDC 55111-153

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 55111-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Limited, 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

Carton1 (Carton1)

Ondansetron Tablets USP 4 mg film-coated tablet carton showing a unit-dose package of 3 tablets (1 blister card). The box includes storage instructions, unit-dose warnings, and manufacturer details for Dr. Reddy's Laboratories Limited, India. The NDC number 55111-153-13 is visible.*

FDA Label Image

Carton2 (Carton2)

Ondansetron Tablets USP 8 mg film-coated tablets carton containing 3 tablets (1 blister card with 3 unit-dose tablets) for oral use. The labeling includes storage instructions, dosage notice, and manufacturer details: Dr. Reddy's Laboratories Limited, India. The carton prominently displays the proprietary name, strength, and labeler.*

FDA Label Image

Carton4

Ondansetron Tablets, USP 24 mg film-coated oral tablets in a unit-dose blister card package. The label indicates a single tablet per unit dose, with storage instructions at 20°-25°C and a warning that the package is not child-resistant. Manufactured by Dr. Reddy's Laboratories Limited, India, with the National Drug Code (NDC) 55111-156-11 shown.*

FDA Label Image

Container1 (Container1)

Label for Ondansetron Tablets, USP 4 mg oral film-coated tablets by Dr. Reddy's Laboratories Limited. The label states a package size of 30 tablets and includes the NDC 55111-153-30. It also features dosage information, storage instructions, and a barcode.*

FDA Label Image

Container2 (Container2)

ONDANSETRON 8 mg film-coated tablets packaging label showing 30 tablets per container. The label includes the proprietary name Ondansetron Tablets, USP, strength 8 mg, and identifies Dr. Reddy's Laboratories Limited as the labeler. It includes a barcode and storage instructions to keep the product at 20-25°C (68-77°F) and in a tightly closed, light-resistant container.*

FDA Label Image

Container4

ONDANSETRON 24 mg film-coated tablets label. The packaging indicates 30 tablets in the bottle from Dr. Reddy's Laboratories Limited. The label includes the active ingredient information, storage instructions, barcode, and manufacturer details. The product is prescription only (Rx Only).*

FDA Label Image

Structure (Structure)

Chemical structure of ondansetron hydrochloride dihydrate, the active ingredient in ONDANSETRON tablets by Dr. Reddy's Laboratories Limited.*

* 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.