NDC 21695-259 Ciprofloxacin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-259 - Ciprofloxacin Hydrochloride
Product Packages
NDC Code 21695-259-05
Package Description: 5 mL in 1 BOTTLE, PLASTIC
NDC Code 21695-259-10
Package Description: 10 mL in 1 BOTTLE, PLASTIC
NDC Code 21695-259-25
Package Description: 2.5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 21695-259?
What are the uses for Ciprofloxacin Hydrochloride?
Which are Ciprofloxacin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CIPROFLOXACIN HYDROCHLORIDE (UNII: 4BA73M5E37)
- CIPROFLOXACIN (UNII: 5E8K9I0O4U) (Active Moiety)
Which are Ciprofloxacin Hydrochloride 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 ACETATE (UNII: 4550K0SC9B)
- ACETIC ACID (UNII: Q40Q9N063P)
- MANNITOL (UNII: 3OWL53L36A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ciprofloxacin Hydrochloride?
- RxCUI: 309307 - ciprofloxacin HCl 0.3 % Ophthalmic Solution
- RxCUI: 309307 - ciprofloxacin 3 MG/ML Ophthalmic Solution
- RxCUI: 309307 - ciprofloxacin 0.3 % Ophthalmic Solution
- RxCUI: 309307 - ciprofloxacin 3 MG/ML (as ciprofloxacin hydrochloride 3.5 MG/ML) Ophthalmic Solution
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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".