NDC 0065-0660 Iopidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0065 - Alcon Laboratories, Inc.
- 0065-0660 - Iopidine
Product Packages
NDC Code 0065-0660-10
Package Description: 12 POUCH in 1 CARTON / 2 VIAL, SINGLE-USE in 1 POUCH / .1 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 0065-0660?
What are the uses for Iopidine?
Which are Iopidine UNII Codes?
The UNII codes for the active ingredients in this product are:
- APRACLONIDINE HYDROCHLORIDE (UNII: D2VW67N38H)
- APRACLONIDINE (UNII: 843CEN85DI) (Active Moiety)
Which are Iopidine 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 CHLORIDE (UNII: 451W47IQ8X)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Iopidine?
- RxCUI: 211020 - IOPIDINE 1 % Ophthalmic Solution
- RxCUI: 211020 - apraclonidine 10 MG/ML Ophthalmic Solution [Iopidine]
- RxCUI: 211020 - Iopidine 1 % Ophthalmic Solution
- RxCUI: 211020 - Iopidine 10 MG/ML (apraclonidine hydrochloride 11.5 MG/ML) Ophthalmic Solution
- RxCUI: 211020 - Iopidine 10 MG/ML Ophthalmic Solution
* Please review the disclaimer below.
Patient Education
Apraclonidine Ophthalmic
Apraclonidine 0.5% eye drops are used for the short-term treatment of glaucoma (a condition that can cause damage to the optic nerve and vision loss, usually due to increased pressure in the eye) in people who are taking other medications for this condition and still have increased pressure in the eye. Apraclonidine 1% eye drops are used to prevent or reduce increased pressure in the eye during and after certain types of laser eye surgery. Apraclonidine is in a class of medications called alpha-2-adrenergic agonists. It lowers the pressure in the eye by decreasing the amount of fluid produced within the eye.
[Learn More]
* Please review the disclaimer below.
[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".