Ondansetron
Product Images NDC 21695-380

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 21695-380). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp., 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

Ondansetron 4mg Label (Ondansetron Sandoz)

Ondansetron ODT 4 mg tablets packaging label, supplied by Rebel Distributors Corp. The label indicates 30 orally disintegrating tablets, each containing 4 mg of Ondansetron base. It is marked RX Only and includes instructions for storage and distribution by Physician Partner in Thousand Oaks, CA.*

FDA Label Image

Structural Formula (B0f74819 9fd5 432a 821c 8216b1f1df83 01)

Chemical structure of Ondansetron, showing specific aromatic and heterocyclic ring structures with attached methyl groups and a carbonyl group.*

FDA Label Image

Ondansetron 4 mg 100s (B0f74819 9fd5 432a 821c 8216b1f1df83 02)

Ondansetron Orally Disintegrating Tablets USP 4 mg, package label for 100 tablets. The label indicates the active ingredient as Ondansetron base 4 mg per tablet. The product is distributed by Sandoz Inc. and manufactured by Suncoz Private Ltd. Storage instructions include keeping the product at 20-25°C (68-77°F) in a controlled room temperature environment, protected from light and moisture.*

FDA Label Image

Ondansetron 4 mg Catron (B0f74819 9fd5 432a 821c 8216b1f1df83 03)

Ondansetron Orally Disintegrating Tablets, USP 4 mg label by Rebel Distributors Corp. The label indicates a package containing 30 tablets in 3 blister cards of 10 tablets each. The label includes usage instructions, storage conditions, and the Sandoz logo with product NDC 21695-380.*

FDA Label Image

Ondansetron 4 mg Blister (B0f74819 9fd5 432a 821c 8216b1f1df83 04)

Packaging label for Ondansetron Orally Disintegrating Tablets, USP by Rebel Distributors Corp. The label includes multiple barcode panels and text blocks displaying the product name, dosage form, and labeler information. The layout is arranged for labeling multiple packages containing the Ondansetron tablets.*

FDA Label Image

Ondansetron Odt 8 mg 100s (B0f74819 9fd5 432a 821c 8216b1f1df83 05)

Ondansetron Orally Disintegrating Tablets USP 8 mg tablet label from Sandoz, showing a pack size of 100 tablets. The label includes usage instructions, storage conditions, warnings about phenylalanine content, and distribution information by Sandoz Inc., Princeton, NJ. The label also notes the product NDC and manufacturer.*

FDA Label Image

Ondansetron 8 mg Carton 10 Tablets (B0f74819 9fd5 432a 821c 8216b1f1df83 06)

Ondansetron Orally Disintegrating Tablets, USP 8 mg carton label by Rebel Distributors Corp. The label states the product strength as 8 mg and includes directions that the package contains 10 tablets (one blister card with 10 tablets). The label shows the Sandoz logo and mentions it is for prescription use only (Rx only). Storage and handling instructions are included, along with the NDC number 21695-380.*

FDA Label Image

Ondansetron 8 mg Carton 30 Tablets (B0f74819 9fd5 432a 821c 8216b1f1df83 07)

Ondansetron Orally Disintegrating Tablets USP 8 mg carton label showing 30 tablets (10 blister cards each containing 10 tablets). The label includes directions that the product is Rx only, manufactured by Sandoz under labeler Rebel Distributors Corp., and features branding and dosage details.*

FDA Label Image

Ondansetron 8 mg Blister (B0f74819 9fd5 432a 821c 8216b1f1df83 08)

Ondansetron Oral Dispersing Tablet USP 8 mg packaging label from Rebel Distributors Corp. The label shows multiple instances of the product name, strength, tablet form, and a barcode with product and lot number areas, arranged in a repeating pattern on a single sheet.*

* 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.