Product Images Ondansetron

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 4 images provide visual information about the product associated with Ondansetron NDC 51655-008 by Northwind Pharmaceuticals, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Label - 51655 008 20

Label - 51655 008 20

This is a prescription medication with NDC 51655-008-20, containing 20 orally disintegrating tablets of Ondansetron, USP. The tablets should not be removed from the blister pack until immediately before use, which should follow the dosage specified in the package insert. The medication must be stored in its original container at temperatures between 20° - 25°C (68° - 77°F) which constitutes USP controlled room temperature. Phenylketonurics, who are sensitive to Phenylalanine, should not take this medication. This product meets USP disintegration test 2 and each of the 20 tablets contains 4mg of ondansetron. The packaging material should not be opened if torn, broken or missing. The medication should be kept out of the reach of children and provided in child-resistant containers for outpatient use. This particular package was repackaged by Northwind Pharmaceuticals in Indianapolis, IN 46203, with a 0000000000 lot and an expiration date of 00/00/0000.*

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* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.