NDC Package 0065-0660-10 Iopidine

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package 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 Code:

0065-0660

Proprietary Name:

Iopidine

Usage Information:

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.

11-Digit NDC Billing Format:

00065066010

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

1 EA

NDC to RxNorm Crosswalk:

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

Labeler Name:

Alcon Laboratories, Inc.

Sample Package:

Start Marketing Date:

05-15-1988

Listing Expiration Date:

12-31-2022

Exclude Flag:

Code Structure:

0065 - Alcon Laboratories, Inc.
- 0065-0660 - Iopidine
  - 0065-0660-10 - 12 POUCH in 1 CARTON / 2 VIAL, SINGLE-USE in 1 POUCH / .1 mL in 1 VIAL, SINGLE-USE

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0065-0660-10?

The NDC Packaged Code 0065-0660-10 is assigned to a package of 12 pouch in 1 carton / 2 vial, single-use in 1 pouch / .1 ml in 1 vial, single-use of Iopidine, labeled by Alcon Laboratories, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 0065-0660 included in the NDC Directory?

No, Iopidine with product code 0065-0660 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Alcon Laboratories, Inc. on May 15, 1988 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0065-0660-10?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 0065-0660-10?

The 11-digit format is 00065066010. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
4-4-2	0065-0660-10	5-4-2	00065-0660-10

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