NDC 21695-628 Tobradex
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What is NDC 21695-628?
What are the uses for Tobradex?
Which are Tobradex UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOBRAMYCIN (UNII: VZ8RRZ51VK)
- TOBRAMYCIN (UNII: VZ8RRZ51VK) (Active Moiety)
- DEXAMETHASONE (UNII: 7S5I7G3JQL)
- DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
Which are Tobradex 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:
- CHLOROBUTANOL (UNII: HM4YQM8WRC)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Tobradex?
- RxCUI: 208821 - TobraDex 0.3 % / 0.1 % Ophthalmic Ointment
- RxCUI: 208821 - dexamethasone 0.001 MG/MG / tobramycin 0.003 MG/MG Ophthalmic Ointment [Tobradex]
- RxCUI: 208821 - Tobradex (tobramycin 0.3 % / dexamethasone 0.1 % ) Ophthalmic Ointment
- RxCUI: 309682 - tobramycin 0.3 % / dexAMETHasone 0.1 % Ophthalmic Ointment
- RxCUI: 309682 - dexamethasone 0.001 MG/MG / tobramycin 0.003 MG/MG Ophthalmic Ointment
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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".