NDC 69639-104 Aloxi
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Product Details
What is NDC 69639-104?
What are the uses for Aloxi?
Which are Aloxi UNII Codes?
The UNII codes for the active ingredients in this product are:
- PALONOSETRON HYDROCHLORIDE (UNII: 23310D4I19)
- PALONOSETRON (UNII: 5D06587D6R) (Active Moiety)
Which are Aloxi 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:
- CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
What is the NDC to RxNorm Crosswalk for Aloxi?
- RxCUI: 805448 - palonosetron 0.5 MG Oral Capsule
- RxCUI: 805448 - palonosetron 0.5 MG (palonosetron hydrochloride 0.056 MG) Oral Capsule
- RxCUI: 805451 - Aloxi 0.5 MG Oral Capsule
- RxCUI: 805451 - palonosetron 0.5 MG Oral Capsule [Aloxi]
- RxCUI: 805451 - Aloxi 0.5 MG (palonosetron hydrochloride 0.056 MG) Oral Capsule
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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".