NDC 63629-2517 Alosetron
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63629 - Bryant Ranch Prepack
- 63629-2517 - Alosetron
Product Characteristics
Product Packages
NDC Code 63629-2517-1
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 63629-2517?
What are the uses for Alosetron?
Which are Alosetron UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOSETRON HYDROCHLORIDE (UNII: 2F5R1A46YW)
- ALOSETRON (UNII: 13Z9HTH115) (Active Moiety)
Which are Alosetron 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Alosetron?
- RxCUI: 403975 - alosetron HCl 0.5 MG Oral Tablet
- RxCUI: 403975 - alosetron 0.5 MG Oral Tablet
- RxCUI: 403975 - alosetron 0.5 MG (as alosetron HCl 0.562 MG) Oral Tablet
* Please review the disclaimer below.
Patient Education
Alosetron
Alosetron is used to treat diarrhea, pain, cramps, and the feeling of an urgent need to have bowel movements caused by irritable bowel syndrome (IBS; a condition that causes stomach pain, bloating, constipation, and diarrhea) in women who have diarrhea as their main symptom and have not been helped by other treatments. Alosetron is in a class of medications called 5-HT3 receptor antagonists. Alosetron works by slowing the movement of stool (bowel movements) through the intestines.
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* 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".