NDC 52268-550 Suflave
Polyethylene Glycol 3350,Sodium Sulfate,Potassium Chloride,Magnesium Sulfate,And Sodium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 52268-550?
What are the uses for Suflave?
Which are Suflave UNII Codes?
The UNII codes for the active ingredients in this product are:
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
Which are Suflave 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:
- ADVANTAME (UNII: 3ZA6810AWX)
- NEOTAME (UNII: VJ597D52EX)
- MALIC ACID (UNII: 817L1N4CKP)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Suflave?
- RxCUI: 2641142 - polyethylene glycol 3350 178.7 GM / potassium chloride 1.12 GM / magnesium sulfate 0.9 GM / sodium chloride 0.5 GM / sodium sulfate 7.3 GM Powder for Oral Solution
- RxCUI: 2641142 - magnesium sulfate 900 MG / polyethylene glycol 3350 179000 MG / potassium chloride 1120 MG / sodium chloride 500 MG / sodium sulfate 7300 MG Powder for Oral Solution
- RxCUI: 2641142 - magnesium sulfate 900 MG / polyethylene glycol 3350 179000 MG / K+ chloride 1120 MG / NaCl 500 MG / sodium sulfate 7300 MG Powder for Oral Solution
- RxCUI: 2641142 - magnesium sulfate 900 MG / polyethylene glycol 3350 179000 MG / Pot chloride 1120 MG / NaCl 500 MG / sodium sulfate 7300 MG Powder for Oral Solution
- RxCUI: 2641143 - {2 (magnesium sulfate 900 MG / polyethylene glycol 3350 179000 MG / potassium chloride 1120 MG / sodium chloride 500 MG / sodium sulfate 7300 MG Powder for Oral Solution) } Pack
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".