NDC 54868-5242 Prednisolone Sodium Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5242 - Prednisolone Sodium Phosphate
Product Characteristics
Product Packages
NDC Code 54868-5242-0
Package Description: 237 mL in 1 BOTTLE
NDC Code 54868-5242-1
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 54868-5242?
What are the uses for Prednisolone Sodium Phosphate?
Which are Prednisolone Sodium Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- PREDNISOLONE SODIUM PHOSPHATE (UNII: IV021NXA9J)
- PREDNISOLONE (UNII: 9PHQ9Y1OLM) (Active Moiety)
Which are Prednisolone 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:
- CORN SYRUP (UNII: 9G5L16BK6N)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Prednisolone Sodium Phosphate?
- RxCUI: 283077 - prednisoLONE sodium phosphate 15 MG in 5 mL Oral Solution
- RxCUI: 283077 - prednisolone 3 MG/ML Oral Solution
- RxCUI: 283077 - prednisolone 15 MG (as prednisolone sodium phosphate 20.2 MG) per 5 ML Oral Solution
- RxCUI: 283077 - prednisolone 15 MG per 5 ML Oral Solution
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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".