Ondansetron Hydrochloride
Product Images NDC 54868-5738

3 FDA label images from Physicians Total Care, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 54868-5738). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Ondansetron Tablets-4mg Package Label (4mg Package Label)

Ondansetron Tablets-4mg Package Label (4mg Package Label)
ONDANSETRON HYDROCHLORIDE 4 MG tablets package label from Physicians Total Care, Inc. The label states a count of 10 tablets and includes a caution that federal law prohibits dispensing without a prescription. Additional information includes dosage instructions, storage directions, lot number, and expiration date.*
FDA Label Image

Ondansetron Tablets-8mg Package Label (8mg Package Label)

Ondansetron Tablets-8mg Package Label (8mg Package Label)
ONDANSETRON HYDROCHLORIDE 8 MG tablet bottle label from Physicians Total Care, Inc., containing 15 tablets. The label includes regulatory information, dosage form, strength, lot number, expiration date, barcode, and federal caution about prescription dispensing.*
FDA Label Image

Ondansetron-structure (Ondansetron Structure)

Ondansetron-structure (Ondansetron Structure)
Chemical structure of ondansetron hydrochloride dihydrate, showing the molecular arrangement including an indole ring, a ketone group, and a methylated imidazole ring with hydrochloride and two water molecules of hydration.*

* 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.