NDC 68071-4775 Gentamicin Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4775 - Gentamicin Sulfate
Product Packages
NDC Code 68071-4775-5
Package Description: 5 mL in 1 BOTTLE
Product Details
What is NDC 68071-4775?
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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- TYLOXAPOL (UNII: Y27PUL9H56)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
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
* Please review the disclaimer below.
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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* 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".