NDC 15631-2372 Bio-combination 17
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 15631-2372-0
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 15631-2372-1
Package Description: 4 TABLET in 1 BLISTER PACK
NDC Code 15631-2372-2
Package Description: 50 TABLET in 1 CONTAINER
NDC Code 15631-2372-3
Package Description: 100 TABLET in 1 CONTAINER
NDC Code 15631-2372-4
Package Description: 250 TABLET in 1 CONTAINER
NDC Code 15631-2372-5
Package Description: 500 TABLET in 1 CONTAINER
NDC Code 15631-2372-6
Package Description: 1000 TABLET in 1 CONTAINER
NDC Code 15631-2372-7
Package Description: 10000 TABLET in 1 CONTAINER
Product Details
What is NDC 15631-2372?
What are the uses for Bio-combination 17?
Which are Bio-combination 17 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
Which are Bio-combination 17 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 (UNII: J2B2A4N98G)
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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".