NDC 68071-4672 Ciprofloxacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4672 - Ciprofloxacin
Product Packages
NDC Code 68071-4672-3
Package Description: 2.5 mL in 1 BOTTLE
Product Details
What is NDC 68071-4672?
What are the uses for Ciprofloxacin?
Which are Ciprofloxacin 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 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:
- SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0)
- ACETIC ACID (UNII: Q40Q9N063P)
- MANNITOL (UNII: 3OWL53L36A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Ciprofloxacin?
- 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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Patient Education
Ciprofloxacin Ophthalmic
Ciprofloxacin ophthalmic solution is used to treat bacterial infections of the eye including conjunctivitis (pinkeye; infection of the membrane that covers the outside of the eyeball and the inside of the eyelid) and corneal ulcers (infection and loss of tissue in the clear front part of the eye). Ciprofloxacin ophthalmic ointment is used to treat conjunctivitis. Ciprofloxacin 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".