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  5. NDC Package Code: 82667-600-05 Maxidex

NDC Package 82667-600-05 Maxidex

Dexamethasone For Suspension Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
82667-600-05
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
82667-600
Proprietary Name:
Maxidex
Non-Proprietary Name:
Dexamethasone
Substance Name:
Dexamethasone
Usage Information:
This medication is used to treat certain eye conditions due to inflammation or injury. Dexamethasone works by relieving symptoms such as swelling, redness, and itching. It belongs to a class of drugs known as corticosteroids. This medication may also be used to treat swelling, redness, and itching of the outer ear due to inflammatory conditions.
11-Digit NDC Billing Format:
82667060005
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Harrow Eye, Llc
Dosage Form:
For Suspension - A product, usually a solid, intended for suspension prior to administration.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Active Ingredient(s):
DEXAMETHASONE 1 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA013422
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-07-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 82667-600-05?

The NDC Packaged Code 82667-600-05 is assigned to a package of 1 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic of Maxidex, a human prescription drug labeled by Harrow Eye, Llc. The product's dosage form is for suspension and is administered via ophthalmic form.

Is NDC 82667-600 included in the NDC Directory?

Yes, Maxidex with product code 82667-600 is active and included in the NDC Directory. The product was first marketed by Harrow Eye, Llc on April 07, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 82667-600-05?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 82667-600-05?

The 11-digit format is 82667060005. 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 5-3-2 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-282667-600-055-4-282667-0600-05