NDC 50090-3091 Moxifloxacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3091 - Moxifloxacin
Product Packages
NDC Code 50090-3091-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 3 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50090-3091?
What are the uses for Moxifloxacin?
Which are Moxifloxacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609)
- MOXIFLOXACIN (UNII: U188XYD42P) (Active Moiety)
Which are Moxifloxacin 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)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Moxifloxacin?
- RxCUI: 403818 - moxifloxacin HCl 0.5 % Ophthalmic Solution
- RxCUI: 403818 - moxifloxacin 5 MG/ML Ophthalmic Solution
- RxCUI: 403818 - moxifloxacin (as moxifloxacin HCl) 0.5 % Ophthalmic Solution
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Patient Education
Moxifloxacin Ophthalmic
Moxifloxacin ophthalmic solution is used to treat bacterial conjunctivitis (pink eye; infection of the membrane that covers the outside of the eyeballs and the inside of the eyelids). Moxifloxacin is in a class of antibiotics called fluoroquinolones. 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".