NDC 46287-024 Potassium Phosphates
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 46287 - Cmp Pharma, Inc.
- 46287-024 - Potassium Phosphates
Product Packages
NDC Code 46287-024-10
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON / 15 mL in 1 VIAL, SINGLE-DOSE
NDC Code 46287-024-15
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON / 15 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 46287-024?
What are the uses for Potassium Phosphates?
Which are Potassium Phosphates 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 PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
Which are Potassium Phosphates 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)
What is the NDC to RxNorm Crosswalk for Potassium Phosphates?
- RxCUI: 2205512 - potassium phosphates (phosphorus 45 MMOL / potassium 71 MEQ) in 15 ML Injection
- RxCUI: 2205512 - 15 ML dibasic potassium phosphate 300 MG/ML / monobasic potassium phosphate 175 MG/ML Injection
- RxCUI: 2205512 - 15 ML Dibasic K+ phosphate 300 MG/ML / Monobasic K+ phosphate 175 MG/ML Injection
- RxCUI: 2205512 - 15 ML Dibasic Pot phosphate 300 MG/ML / Monobasic Pot phosphate 175 MG/ML Injection
- RxCUI: 2205512 - phosphorus 45 MMOL / potassium 71 MEQ per 15 ML Injection
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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".