NDC 21695-380 Ondansetron
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp.
- 21695-380 - Ondansetron
Product Characteristics
Product Packages
NDC Code 21695-380-30
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE
Product Details
What is NDC 21695-380?
What are the uses for Ondansetron?
Which are Ondansetron UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONDANSETRON (UNII: 4AF302ESOS)
- 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:
- ASPARTAME (UNII: Z0H242BBR1)
- CALCIUM STEARATE (UNII: 776XM7047L)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
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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".