NDC 51655-800 Ondansetron Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 51655-800?
What are the uses for Ondansetron Hydrochloride?
Which are Ondansetron Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONDANSETRON HYDROCHLORIDE (UNII: NMH84OZK2B)
- ONDANSETRON (UNII: 4AF302ESOS) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Ondansetron Hydrochloride?
- RxCUI: 198052 - ondansetron HCl 4 MG Oral Tablet
- RxCUI: 198052 - ondansetron 4 MG Oral Tablet
- RxCUI: 198052 - ondansetron 4 MG (as ondansetron HCl dihydrate 5 MG) Oral Tablet
* Please review the disclaimer below.
Patient Education
Ondansetron
Ondansetron is used to prevent nausea and vomiting caused by cancer chemotherapy, radiation therapy, and surgery. Ondansetron is in a class of medications called serotonin 5-HT3 receptor antagonists. It works by blocking the action of serotonin, a natural substance that may cause nausea and vomiting.
[Learn More]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".