NDC 17478-290 Tobramycin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-290 - Tobramycin
Product Packages
NDC Code 17478-290-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Price per Unit: $1.46427 per ML
Product Details
What is NDC 17478-290?
What are the uses for Tobramycin?
Which are Tobramycin UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOBRAMYCIN (UNII: VZ8RRZ51VK)
- TOBRAMYCIN (UNII: VZ8RRZ51VK) (Active Moiety)
Which are Tobramycin 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:
- BORIC ACID (UNII: R57ZHV85D4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- TYLOXAPOL (UNII: Y27PUL9H56)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SULFURIC ACID (UNII: O40UQP6WCF)
- WATER (UNII: 059QF0KO0R)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for Tobramycin?
- RxCUI: 313415 - tobramycin 0.3 % Ophthalmic Solution
- RxCUI: 313415 - tobramycin 3 MG/ML Ophthalmic Solution
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Patient Education
Tobramycin Ophthalmic
Ophthalmic tobramycin is used to treat eye infections. Tobramycin is in a class of medications called antibiotics. It works by killing bacteria that cause infections.
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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".