NDC 15631-2361 Bio-combination 6
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 15631-2361-0
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 15631-2361-1
Package Description: 4 TABLET in 1 BLISTER PACK
NDC Code 15631-2361-2
Package Description: 50 TABLET in 1 CONTAINER
NDC Code 15631-2361-3
Package Description: 100 TABLET in 1 CONTAINER
NDC Code 15631-2361-4
Package Description: 250 TABLET in 1 CONTAINER
NDC Code 15631-2361-5
Package Description: 500 TABLET in 1 CONTAINER
NDC Code 15631-2361-6
Package Description: 1000 TABLET in 1 CONTAINER
NDC Code 15631-2361-7
Package Description: 10000 TABLET in 1 CONTAINER
Product Details
What is NDC 15631-2361?
What are the uses for Bio-combination 6?
Which are Bio-combination 6 UNII Codes?
The UNII codes for the active ingredients in this product are:
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
Which are Bio-combination 6 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)
* 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".