NDC 52565-090 Gentamicin Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52565 - Teligent Pharma, Inc.
- 52565-090 - Gentamicin Sulfate
Product Packages
NDC Code 52565-090-15
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
Price per Unit: $1.36365 per GM
NDC Code 52565-090-30
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
Price per Unit: $0.83344 per GM
Product Details
What is NDC 52565-090?
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:
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PETROLATUM (UNII: 4T6H12BN9U)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Gentamicin Sulfate?
- RxCUI: 310465 - gentamicin sulfate 0.1 % Topical Ointment
- RxCUI: 310465 - gentamicin 0.001 MG/MG Topical Ointment
- RxCUI: 310465 - gentamicin (as gentamicin sulfate) 0.1 % Topical Ointment
- RxCUI: 310465 - gentamicin sulfate 0.001 MG/MG Topical Ointment
* Please review the disclaimer below.
Patient Education
Gentamicin Topical
Topical gentamicin is used in adults and children 1 year of age and older to treat skin infections caused by certain bacteria. Topical gentamicin is in a class of medications called antibiotics. It works by killing bacteria that cause infections.
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* Please review the disclaimer below.
[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".