Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 51655-415

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 51655-415). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

51655-415-04 (51655 415 04)

Ondansetron Hydrochloride 4 mg film-coated tablets label from Northwind Health Company, LLC. The label includes dose information, quantity of 4 tablets, and prescription-only status. It also lists lot number, expiration date, storage instructions, and manufacturer details for Citron Pharma LLC.*

FDA Label Image

51655-415-43 (51655 415 43)

Ondansetron 4 mg film-coated tablets packaging label showing a 3-tablet unit dosage. The label includes the product name Ondansetron 4 mg, prescription status (Rx Only), lot number, expiration date (12/2021), and manufacturer details from Northwind Health Company, LLC. Additional text includes storage instructions and medication guide availability information.*

FDA Label Image

51655-415-53 (51655 415 53)

Ondansetron Hydrochloride 4 mg film-coated oral tablets carton label from Northwind Health Company, LLC. Package contains 10 tablets labeled Rx only. Includes lot number UT25310014 and expiration date 07/2021. Manufacturing details and storage instructions are also visible.*

FDA Label Image

51655-415-54 (51655 415 54)

Ondansetron Hydrochloride 4 mg film-coated tablets label by Northwind Health Company, LLC. The label indicates a bottle containing 15 tablets, prescription only. It includes lot number UT25310013 and expiration date 07/2021, with storage instructions at 68-77 degrees F. The label shows dosage information and a barcode.*

FDA Label Image

51655-415-55 (51655 415 55)

Ondansetron Hydrochloride 4 mg film-coated tablets label from Northwind Health Company, LLC. The label shows a blister pack with 5 tablets, lot number UT25311012, expiration date 07/2021, and dosing information stating each tablet contains 4 mg Ondansetron USP. Manufacturer and distributor information are included along with storage instructions.*

FDA Label Image

51655-415-87 (51655 415 87)

Ondansetron Hydrochloride 4 mg film-coated tablets label from Northwind Health Company, LLC. The label indicates a package of 6 tablets for oral use, with prescription-only status. It includes lot number and expiration date (12/2021), dosing and storage instructions, and manufacturer contact information.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride dihydrate, showing its molecular arrangement with characteristic rings and functional groups.*

* 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.