NDC 11695-1431 Prednisolone Sodium Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 11695-1431?
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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Prednisolone Sodium Phosphate?
- RxCUI: 314165 - prednisoLONE sodium phosphate 1 % Ophthalmic Solution
- RxCUI: 314165 - prednisolone 10 MG/ML Ophthalmic Solution
- RxCUI: 314165 - prednisolone sodium phosphate 1 % Ophthalmic Solution
* Please review the disclaimer below.
[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".