NDC 54868-6301 Bromday
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6301 - Bromday
Product Packages
NDC Code 54868-6301-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 1.7 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 54868-6301?
What are the uses for Bromday?
Which are Bromday UNII Codes?
The UNII codes for the active ingredients in this product are:
- BROMFENAC SODIUM (UNII: 8ECV571Y37)
- BROMFENAC (UNII: 864P0921DW) (Active Moiety)
Which are Bromday 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)
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bromday?
- RxCUI: 1020510 - Bromday 0.09 % Ophthalmic Solution
- RxCUI: 1020510 - bromfenac 0.9 MG/ML Ophthalmic Solution [Bromday]
- RxCUI: 578018 - bromfenac 0.09 % Ophthalmic Solution
- RxCUI: 578018 - bromfenac 0.9 MG/ML Ophthalmic Solution
- RxCUI: 578018 - bromfenac 0.9 MG/ML (bromfenac sodium 1.035 MG/ML) Ophthalmic 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".