NDC 68151-2193 K Phos Original
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-2193 - K Phos
Product Characteristics
Product Packages
NDC Code 68151-2193-0
Package Description: 1 TABLET, SOLUBLE in 1 PACKAGE
Product Details
What is NDC 68151-2193?
What are the uses for K Phos Original?
Which are K Phos Original UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are K Phos Original 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for K Phos Original?
- RxCUI: 1101775 - monobasic potassium phosphate 0.0408 MEQ/ML Oral Solution
- RxCUI: 1101775 - Monobasic K+ phosphate 0.0408 MEQ/ML Oral Solution
- RxCUI: 1101775 - Monobasic Pot phosphate 0.0408 MEQ/ML Oral Solution
- RxCUI: 1101778 - K-Phos 500 MG Tablet for Oral Solution
- RxCUI: 1101778 - monobasic potassium phosphate 0.0408 MEQ/ML Oral Solution [K-Phos]
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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".