NDC 21695-834 Ondansetron Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-834 - Ondansetron Hydrochloride
Product Characteristics
Product Packages
NDC Code 21695-834-04
Package Description: 4 TABLET, FILM COATED in 1 BOTTLE
NDC Code 21695-834-12
Package Description: 12 TABLET, FILM COATED in 1 BOTTLE
NDC Code 21695-834-15
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE
NDC Code 21695-834-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 21695-834?
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)
Which are Ondansetron Hydrochloride 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 LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
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
- RxCUI: 312086 - ondansetron HCl 8 MG Oral Tablet
- RxCUI: 312086 - ondansetron 8 MG Oral Tablet
* 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".