NDC 21695-654 Zonisamide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GRAY (C48324 - LIGHT GRAY OPAQUE)
Code Structure Chart
Product Details
What is NDC 21695-654?
What are the uses for Zonisamide?
Which are Zonisamide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZONISAMIDE (UNII: 459384H98V)
- ZONISAMIDE (UNII: 459384H98V) (Active Moiety)
Which are Zonisamide 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Zonisamide?
- RxCUI: 314285 - zonisamide 100 MG Oral Capsule
- RxCUI: 403967 - zonisamide 50 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".