NDC 0065-0660 Iopidine

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0065-0660
Proprietary Name:
Iopidine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Alcon Laboratories, Inc.
Labeler Code:
0065
Start Marketing Date: [9]
05-15-1988
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 0065-0660 is assigned by the FDA to the product Iopidine which is product labeled by Alcon Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0065-0660-10 12 pouch in 1 carton / 2 vial, single-use in 1 pouch / .1 ml in 1 vial, single-use. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Iopidine?

This medication is used to treat or prevent high pressure inside the eye that may occur during and after laser eye surgery. Decreasing high pressure inside the eye may help to prevent decreased vision or blindness in the eye treated by laser surgery. Apraclonidine is thought to work by decreasing the amount of fluid within the eye.

Which are Iopidine UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Iopidine?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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.
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Product Footnotes

[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".