NDC 54868-6282 Besivance
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What is NDC 54868-6282?
What are the uses for Besivance?
Which are Besivance UNII Codes?
The UNII codes for the active ingredients in this product are:
- BESIFLOXACIN (UNII: BFE2NBZ7NX)
- BESIFLOXACIN (UNII: BFE2NBZ7NX) (Active Moiety)
Which are Besivance 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)
- POLYCARBOPHIL (UNII: W25LM17A4W)
- MANNITOL (UNII: 3OWL53L36A)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Besivance?
- RxCUI: 850305 - besifloxacin 0.6 % Ophthalmic Suspension
- RxCUI: 850305 - besifloxacin 6 MG/ML Ophthalmic Suspension
- RxCUI: 850309 - Besivance 0.6 % Ophthalmic Suspension
- RxCUI: 850309 - besifloxacin 6 MG/ML Ophthalmic Suspension [Besivance]
- RxCUI: 850309 - Besivance 6 MG/ML Ophthalmic Suspension
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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".