ondansetron 8 MG Disintegrating Oral Tablet
INDICATIONS AND USAGE prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥ 50 mg/m 2 . prevention of nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy. prevention of nausea and vomiting associated with radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen. prevention of postoperative nausea and/or vomiting. As with other antiemetics, routine prophylaxis is not recommended for patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively. In patients where nausea and/or vomiting must be avoided postoperatively, ondansetron orally disintegrating tablets are recommended even where the incidence of postoperative nausea and/or vomiting is low.
Sun Pharmaceutical Industries Limited
OVAL WHITE 241
241 OVAL WHITE
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HOW SUPPLIED Ondansetron orally disintegrating tablets, 4 mg (as 4 mg ondansetron base) are white to off white, oval, uncoated tablets debossed with “240” on one side, plain on the other side. Bottle pack of 30 tablets with Child Resistant Cap (NDC 62756-240-83) Unit dose packs of 30 tablets (NDC 62756-240-64) Ondansetron orally disintegrating tablets, 8 mg (as 8 mg ondansetron base) are white to off white, oval, uncoated tablets debossed with “241” on one side, plain on the other side. Bottle pack of 30 tablets with Child Resistant Cap (NDC 62756-356-83) Unit dose packs of 30 tablets (NDC 62756-356-64) Unit dose packs of 10 tablets (NDC 62756-356-66) Store between 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
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