NDC 54868-0634 Blephamide
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Product Details
What is NDC 54868-0634?
What are the uses for Blephamide?
Which are Blephamide UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ)
- SULFACETAMIDE (UNII: 4965G3J0F5) (Active Moiety)
- PREDNISOLONE ACETATE (UNII: 8B2807733D)
- PREDNISOLONE (UNII: 9PHQ9Y1OLM) (Active Moiety)
Which are Blephamide 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)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- WATER (UNII: 059QF0KO0R)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Blephamide?
- RxCUI: 1012015 - sulfacetamide sodium 10 % / prednisoLONE acetate 0.2 % Ophthalmic Suspension
- RxCUI: 1012015 - prednisolone acetate 2 MG/ML / sulfacetamide sodium 100 MG/ML Ophthalmic Suspension
- RxCUI: 1012015 - prednisolone acetate 0.2 % / sulfacetamide sodium 10 % Ophthalmic Suspension
- RxCUI: 1012017 - BLEPHAMIDE 10 % / 0.2 % Ophthalmic Suspension
- RxCUI: 1012017 - prednisolone acetate 2 MG/ML / sulfacetamide sodium 100 MG/ML Ophthalmic Suspension [Blephamide]
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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".