NDC Package 70069-232-01 Brimonidine Tartrate

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

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:
70069-232-01
Package Description:
1 BOTTLE in 1 CARTON / 10 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Brimonidine Tartrate
Non-Proprietary Name:
Brimonidine Tartrate
Substance Name:
Brimonidine Tartrate
Usage Information:
This medication is used to treat open-angle glaucoma or high fluid pressure in the eye. Lowering high fluid pressure in the eye reduces the risk of vision loss, nerve damage, or blindness. This medication lowers pressure by allowing better fluid drainage from within the eye and also by reducing the amount of fluid formed in the eye. It is known as an alpha agonist. This drug is not recommended for use in children less than 2 years of age due to an increased risk of serious side effects such as very slowed breathing. Ask the doctor or pharmacist for details.
11-Digit NDC Billing Format:
70069023201
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 861200 - brimonidine tartrate 0.2 % Ophthalmic Solution
  • RxCUI: 861200 - brimonidine tartrate 2 MG/ML Ophthalmic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Somerset Therapeutics, Llc
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA208992
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-11-2019
    Listing Expiration Date:
    12-31-2024
    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 70069-232-01?

    The NDC Packaged Code 70069-232-01 is assigned to a package of 1 bottle in 1 carton / 10 ml in 1 bottle of Brimonidine Tartrate, a human prescription drug labeled by Somerset Therapeutics, Llc. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 70069-232 included in the NDC Directory?

    Yes, Brimonidine Tartrate with product code 70069-232 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on March 11, 2019 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 70069-232-01?

    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 70069-232-01?

    The 11-digit format is 70069023201. 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
    5-3-270069-232-015-4-270069-0232-01