Product Images Ondansetron

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Product Label Images

The following 2 images provide visual information about the product associated with Ondansetron NDC 51655-913 by Northwind Pharmaceuticals, 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 913 53 Master Bottle Label Approval Rev A 01 21

Label - 51655 913 53 Master Bottle Label Approval   Rev A 01 21

NDC 51655-913-53 is a prescription medication composed of Ondansetron Orally Disintegrating Tablets. Each package includes 10 tablets, with a dosage as indicated in the package insert. The medication should be stored in its original container at a temperature range from 20-25°C, with excursions permitted between 15-30°C. It contains Phenylalanine per tablet, and each orally disintegrating tablet contains Ondansetron USP 4mg. The unit-dose blister pack is child-resistant and should only be removed just before usage. The medication must not be used if blisters are torn, broken, or missing. The medication is repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46203, and manufactured by Rising Health LLC, with lot number 0000000000 and expiration date 00/00/0000.*

Chemical Structure - ondansetronod str

Chemical Structure - ondansetronod str

* 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.