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  5. NDC Package Code: 24208-464-10 Brinzolamide

NDC Package 24208-464-10 Brinzolamide

Suspension/ Drops Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
24208-464-10
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 10 mL in 1 BOTTLE, PLASTIC
Product Code:
24208-464
Proprietary Name:
Brinzolamide
Non-Proprietary Name:
Brinzolamide
Substance Name:
Brinzolamide
Usage Information:
Brinzolamide is used to treat high pressure inside the eye due to glaucoma (open angle-type) or other eye diseases (e.g., ocular hypertension). Lowering high pressure inside the eye helps to prevent blindness. This medication works by decreasing the amount of fluid within the eye. It belongs to a class of drugs known as carbonic anhydrase inhibitors.
11-Digit NDC Billing Format:
24208046410
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Bausch & Lomb Incorporated
Dosage Form:
Suspension/ Drops - A suspension which is usually administered in a dropwise fashion.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Active Ingredient(s):
BRINZOLAMIDE 10 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA204884
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-31-2022
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
24208-464-151 BOTTLE, PLASTIC in 1 CARTON / 15 mL in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 24208-464-10?

The NDC Packaged Code 24208-464-10 is assigned to a package of 1 bottle, plastic in 1 carton / 10 ml in 1 bottle, plastic of Brinzolamide, a human prescription drug labeled by Bausch & Lomb Incorporated. The product's dosage form is suspension/ drops and is administered via ophthalmic form.

Is NDC 24208-464 included in the NDC Directory?

Yes, Brinzolamide with product code 24208-464 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on March 31, 2022 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 11-digit format for NDC 24208-464-10?

The 11-digit format is 24208046410. 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
5-3-224208-464-105-4-224208-0464-10