NDC 17856-4091 Ondansetron
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-4091 - Ondansetron
Product Characteristics
Product Packages
NDC Code 17856-4091-3
Package Description: 5 mL in 1 CUP
Product Details
What is NDC 17856-4091?
What are the uses for Ondansetron?
Which are Ondansetron UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONDANSETRON HYDROCHLORIDE (UNII: NMH84OZK2B)
- ONDANSETRON (UNII: 4AF302ESOS) (Active Moiety)
Which are Ondansetron Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- STRAWBERRY (UNII: 4J2TY8Y81V)
What is the NDC to RxNorm Crosswalk for Ondansetron?
- RxCUI: 312085 - ondansetron HCl 4 MG in 5 mL Oral Solution
- RxCUI: 312085 - ondansetron 0.8 MG/ML Oral Solution
- RxCUI: 312085 - ondansetron (as ondansetron HCl dihydrate) 4 MG per 5 ML Oral Solution
- RxCUI: 312085 - ondansetron 4 MG per 5 ML Oral Solution
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[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".