NDC Package 0078-0792-05 Maxitrol

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 discontinued by the firm.

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:

0078-0792-05

Package Description:

5 mL in 1 BOTTLE, PLASTIC

Product Code:

0078-0792

Proprietary Name:

Maxitrol

Usage Information:

This medication is used to treat conditions involving swelling (inflammation) of the eyes and to treat or prevent bacterial eye infections. This product contains neomycin and polymyxin, antibiotics that work by stopping the growth of bacteria. It also contains dexamethasone, an anti-inflammatory corticosteroid that works by reducing swelling. This medication treats/prevents only bacterial eye infections. It will not work for other types of eye infections and may worsen them (e.g., infections caused by viruses, fungi, mycobacteria). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.

11-Digit NDC Billing Format:

00078079205

Billing Unit:

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

NDC to RxNorm Crosswalk:

5 ML

Labeler Name:

Novartis Pharmaceuticals Corporation

Sample Package:

FDA Application Number:

NDA050023

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

11-15-1964

End Marketing Date:

10-31-2024

Listing Expiration Date:

10-31-2024

Exclude Flag:

Code Structure:

0078 - Novartis Pharmaceuticals Corporation
- 0078-0792 - Maxitrol
  - 0078-0792-05 - 5 mL in 1 BOTTLE, PLASTIC

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 0078-0792-05?

The NDC Packaged Code 0078-0792-05 is assigned to a package of 5 ml in 1 bottle, plastic of Maxitrol, labeled by Novartis Pharmaceuticals Corporation. The product's dosage form is and is administered via form.This product is billed per "ML" milliliter and contains an estimated amount of 5 billable units per package.

Is NDC 0078-0792 included in the NDC Directory?

No, Maxitrol with product code 0078-0792 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Novartis Pharmaceuticals Corporation on November 15, 1964 and its listing in the NDC Directory is set to expire on October 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0078-0792-05?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 5.

What is the 11-digit format for NDC 0078-0792-05?

The 11-digit format is 00078079205. 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	0078-0792-05	5-4-2	00078-0792-05

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