NDC 68151-2195 Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-2195 - Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate
Product Characteristics
Product Packages
NDC Code 68151-2195-0
Package Description: 1 TABLET in 1 PACKAGE
Product Details
What is NDC 68151-2195?
What are the uses for Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate?
Which are Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
Which are Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate 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:
- WATER (UNII: 059QF0KO0R)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POVIDONE K30 (UNII: U725QWY32X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE 2910 (15000 MPA.S) (UNII: 288VBX44JC)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Dibasic Sodium Phosphate, Monobasic Potassium Phosphate And Monobasic Sodium Phosphate?
- RxCUI: 200251 - sodium phosphate, dibasic 852 MG / potassium phosphate, monobasic 155 MG / sodium phosphate, monobasic 130 MG Oral Tablet
- RxCUI: 200251 - potassium phosphate 155 MG / sodium phosphate, dibasic 852 MG / sodium phosphate, monobasic 130 MG Oral Tablet
- RxCUI: 200251 - K+ phosphate 155 MG / Sodium Phosphate, Dibasic 852 MG / Sodium Phosphate, Monobasic 130 MG Oral Tablet
- RxCUI: 200251 - Pot phosphate 155 MG / Sodium Phosphate, Dibasic 852 MG / Sodium Phosphate, Monobasic 130 MG Oral Tablet
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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".