NDC 66992-450 Cetraxal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66992 - Wraser Llc
- 66992-450 - Cetraxal
Product Packages
NDC Code 66992-450-14
Package Description: 14 CONTAINER in 1 CARTON / .25 mL in 1 CONTAINER
Product Details
What is NDC 66992-450?
What are the uses for Cetraxal?
Which are Cetraxal UNII Codes?
The UNII codes for the active ingredients in this product are:
- CIPROFLOXACIN HYDROCHLORIDE (UNII: 4BA73M5E37)
- CIPROFLOXACIN (UNII: 5E8K9I0O4U) (Active Moiety)
Which are Cetraxal 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:
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LACTIC ACID (UNII: 33X04XA5AT)
What is the NDC to RxNorm Crosswalk for Cetraxal?
- RxCUI: 848956 - ciprofloxacin HCl 0.2 % Otic Solution
- RxCUI: 848956 - ciprofloxacin 2 MG/ML Otic Solution
- RxCUI: 848956 - ciprofloxacin 0.2 % Otic Solution
- RxCUI: 848960 - Cetraxal 0.2 % Otic Solution
- RxCUI: 848960 - ciprofloxacin 2 MG/ML Otic Solution [Cetraxal]
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Patient Education
Ciprofloxacin Otic
Ciprofloxacin otic solution (Cetraxal) and ciprofloxacin otic suspension (Otiprio) are used to treat outer ear infections in adults and children. Ciprofloxacin otic suspension (Otiprio) is also used in children during ear tube placement surgery to prevent infection or ear drainage. Ciprofloxacin otic is in a class of medications called quinolone 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".