NDC 62756-0130-01
ondansetron hydrochloride 4 mg/1 TABLET, FILM COATED
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NDC
62756-0130-01
Generic Name
ondansetron hydrochloride
Brand Name
ondansetron hydrochloride
Strength
4 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
—
Labeler
Sun Pharmaceutical Industries, Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Ondansetron is indicated for the prevention of nausea and vomiting associated with: highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m 2 . initial and repeat courses of moderately emetogenic cancer chemotherapy. radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen. Ondansetron is also indicated for the prevention of postoperative nausea and/or…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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