NDC 54868-1157 Blephamide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-1157 - Blephamide
Product Packages
NDC Code 54868-1157-0
Package Description: 1 TUBE in 1 CARTON / 3.5 g in 1 TUBE
Product Details
What is NDC 54868-1157?
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:
- PHENYLMERCURIC ACETATE (UNII: OSX88361UX)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
What is the NDC to RxNorm Crosswalk for Blephamide?
- RxCUI: 1011985 - sulfacetamide sodium 10 % / prednisoLONE acetate 0.2 % Ophthalmic Ointment
- RxCUI: 1011985 - prednisolone acetate 0.002 MG/MG / sulfacetamide sodium 0.1 MG/MG Ophthalmic Ointment
- RxCUI: 1011985 - prednisolone acetate 0.2 % / sulfacetamide sodium 10 % Ophthalmic Ointment
- RxCUI: 1011987 - BLEPHAMIDE 10 % / 0.2 % Ophthalmic Ointment
- RxCUI: 1011987 - prednisolone acetate 0.002 MG/MG / sulfacetamide sodium 0.1 MG/MG Ophthalmic Ointment [Blephamide]
* 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".