NDC Package 59390-182-13 Goniotaire

Hypromellose 2906 (4000 Mpa.s) Solution Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

59390-182-13

Package Description:

1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE

Product Code:

59390-182

Proprietary Name:

Goniotaire

Non-Proprietary Name:

Hypromellose 2906 (4000 Mpa.s)

Substance Name:

Hypromellose 2906 (4000 Mpa.s)

Usage Information:

For professional use in gonioscopic examinations.

11-Digit NDC Billing Format:

59390018213

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

RxCUI: 310934 - hypromellose 2.5 % Ophthalmic Solution

RxCUI: 310934 - hypromellose 25 MG/ML Ophthalmic Solution

Product Type:

Human Prescription Drug

Labeler Name:

Altaire Pharmaceuticals Inc.

Dosage Form:

Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Administration Route(s):

Ophthalmic - Administration to the external eye.

Active Ingredient(s):

HYPROMELLOSE 2906 (4000 MPA.S) 25 mg/mL

Sample Package:

Marketing Category:

UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Start Marketing Date:

01-18-2002

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

59390 - Altaire Pharmaceuticals Inc.
- 59390-182 - Goniotaire
  - 59390-182-13 - 1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE

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 59390-182-13?

The NDC Packaged Code 59390-182-13 is assigned to a package of 1 bottle in 1 carton / 15 ml in 1 bottle of Goniotaire, a human prescription drug labeled by Altaire Pharmaceuticals Inc.. The product's dosage form is solution and is administered via ophthalmic form.

Is NDC 59390-182 included in the NDC Directory?

Yes, Goniotaire with product code 59390-182 is active and included in the NDC Directory. The product was first marketed by Altaire Pharmaceuticals Inc. on January 18, 2002 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 59390-182-13?

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 59390-182-13?

The 11-digit format is 59390018213. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	59390-182-13	5-4-2	59390-0182-13

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