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.*
