NDC 57319-347 Neomycin Polymyxin B Sulfates And Dexamethasone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57319 - Phoenix Pharmaceutical, Inc.
- 57319-347 - Neomycin Polymyxin B Sulfates And Dexamethasone
Product Packages
NDC Code 57319-347-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57319-347?
What are the uses for Neomycin Polymyxin B Sulfates And Dexamethasone?
Which are Neomycin Polymyxin B Sulfates And Dexamethasone UNII Codes?
The UNII codes for the active ingredients in this product are:
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- POLYMYXIN B SULFATE (UNII: 19371312D4)
- POLYMYXIN B (UNII: J2VZ07J96K) (Active Moiety)
- DEXAMETHASONE (UNII: 7S5I7G3JQL)
- DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
Which are Neomycin Polymyxin B Sulfates And Dexamethasone 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)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Neomycin Polymyxin B Sulfates And Dexamethasone?
- RxCUI: 309680 - neomycin sulfate 3.5 MG/ML / polymyxin B sulfate 10,000 UNT/mL / dexAMETHasone 0.1 % Ophthalmic Suspension
- RxCUI: 309680 - dexamethasone 1 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Ophthalmic Suspension
- RxCUI: 309680 - dexamethasone 0.1 % / neomycin 0.35 % / polymyxin B 10,000 UNT per ML Ophthalmic Suspension
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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".