Ondansetron Hydrochloride
Product Images NDC 55045-3729

View Photos of 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 55045-3729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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

Ndc 55045-3729-03 (Ndc 55045 3729 03 Caraco)

Ndc 55045-3729-03 (Ndc 55045 3729 03      Caraco)
This is a pharmaceutical package of Ondansetron HCI 4 mg tablets distributed by Caraco Pharmaceutical Laboratories, LTD. The tablets are white oval film-coated and engraved with 130. The package contains 30 tablets, and each tablet contains 5 mg of Ondansetron Hydrochloride Dihydrate equivalent to 4 mg of Ondansetron. The product is dispensed with a tight/light-resistant container and is intended for oral intake every hour, as directed by the physician. The package includes the manufacturer's lot and the product ID, which matches the NDC code 62756-0130-01. The warning label advises to keep the medication out of children's reach, and the medication should be stored at 68°- 77° Fahrenheit. The package is exclusively packaged by Dispensing Solutions in Santa Ana, CA 92704.*
FDA Label Image

Ndc 55045-3817-03 (Ndc 55045 3817 03 Caraco)

Ndc 55045-3817-03 (Ndc 55045 3817 03      Caraco)
This is a label for a product consisting of 30 tablets of Ondansetron HCI 8mg, distributed by Caraco Pharmaceutical Laboratories LTD, with a product ID 700430 and NDC code 55045-3817-03. Each yellow, oval, film-coated tablet is engraved with "131". The recommended dosage and frequency of consumption must be according to a physician’s indications. The tablets must be dispensed in the provided tight and light-resistant container, stored at 68°- 77° F. The label contains RX only and a warning to keep out of children's reach. The drug's manufacturing lot is not specified, and the associated expiration date is indicated as 00-00.*
FDA Label Image

Ondansetron-structure (Ondansetron Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.