NDC 44946-1017 Ludent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44946 - Sancilio & Company Inc
- 44946-1017 - Ludent
Product Characteristics
9 MM
13 MM
SCI;1007
SCI;1004
Product Packages
NDC Code 44946-1017-2
Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
NDC Code 44946-1017-3
Package Description: 120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
NDC Code 44946-1017-6
Package Description: 30 TABLET, CHEWABLE in 1 BLISTER PACK
Product Details
What is NDC 44946-1017?
What are the uses for Ludent?
Which are Ludent UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Ludent 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MALIC ACID (UNII: 817L1N4CKP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- XYLITOL (UNII: VCQ006KQ1E)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Ludent?
- RxCUI: 198215 - fluoride 0.25 MG Chewable Tablet
- RxCUI: 198215 - sodium fluoride 0.55 MG Chewable Tablet
- RxCUI: 198215 - sodium fluoride 0.55 MG (fluoride ion 0.25 MG) Chewable Tablet
- RxCUI: 313036 - sodium fluoride 1.1 MG Chewable Tablet
- RxCUI: 313036 - sodium fluoride 1.1 MG (fluoride ion 0.5 MG) Chewable 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".