Glycophos
NDC 63323-241
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
Glycophos is a UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE-approved product labeled by Fresenius Kabi Usa, Llc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 63323-241 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63323-241
Proprietary Name:
Glycophos
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
63323
Product Label ID:
Marketing Category: [8]
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing Timeline
Start Marketing Date: [9]
05-13-2013
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
I
Code Structure Chart
Product Details
What is NDC 63323-241?
The NDC code 63323-241 is assigned by the FDA to the product Glycophos. This pharmaceutical product is labeled by Fresenius Kabi Usa, Llc and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63323-241-20. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM GLYCEROPHOSPHATE ANHYDROUS (UNII: YP1H63LJ2K)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
Which are the Inactive Ingredients associated 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:
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for this product?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 1423807 - sodium glycerophosphate 4.32 GM (sodium 40 mmol, phosphate 20 mmol) in 20 ML Injection
- RxCUI: 1423807 - 20 ML sodium glycerophosphate 216 MG/ML Injection
- RxCUI: 1423807 - sodium glycerophosphate 4.32 GM (sodium 40 mmol, phosphate 20 mmol) per 20 ML Injection
- RxCUI: 1423812 - Glycophos 4.32 GM (sodium 40 mmol, phosphate 20 mmol) in 20 ML Injection
- RxCUI: 1423812 - 20 ML sodium glycerophosphate 216 MG/ML Injection [Glycophos]
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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
