NDC 17478-283 Gentamicin Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-283 - Gentamicin Sulfate
Product Packages
NDC Code 17478-283-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Price per Unit: $1.06744 per ML
Product Details
What is NDC 17478-283?
What are the uses for Gentamicin Sulfate?
Which are Gentamicin Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- GENTAMICIN SULFATE (UNII: 8X7386QRLV)
- GENTAMICIN (UNII: T6Z9V48IKG) (Active Moiety)
Which are Gentamicin Sulfate 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:
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for Gentamicin Sulfate?
- RxCUI: 310467 - gentamicin sulfate 0.3 % Ophthalmic Solution
- RxCUI: 310467 - gentamicin 3 MG/ML Ophthalmic Solution
- RxCUI: 310467 - gentamicin (as gentamicin sulfate) 0.3 % Ophthalmic Solution
- RxCUI: 310467 - gentamicin sulfate 3 MG/ML Ophthalmic Solution
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Patient Education
Gentamicin Ophthalmic
Ophthalmic gentamicin is used to treat certain eye infections. Gentamicin is in a class of medications called antibiotics. It works by killing the bacteria that cause infection.
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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".