NDC 65862-0188-30
Ondansetron Hydrochloride 8 mg/1 TABLET, FILM COATED
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NDC
65862-0188-30
Generic Name
Ondansetron Hydrochloride
Brand Name
Ondansetron Hydrochloride
Strength
8 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
—
Labeler
Aurobindo Pharma Limited
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Ondansetron tablets are 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 tablets are also indicated for the prevention of postoperative…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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