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  5. NDC Package Code: 70069-711-01 Bepotastine Besilate

NDC Package 70069-711-01 Bepotastine Besilate

Solution 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:
70069-711-01
Package Description:
1 BOTTLE in 1 CARTON / 5 mL in 1 BOTTLE
Product Code:
70069-711
Proprietary Name:
Bepotastine Besilate
Non-Proprietary Name:
Bepotastine Besilate
Substance Name:
Bepotastine Besilate
Usage Information:
This medication is used to treat itching of the eyes due to allergies. Bepotastine is an antihistamine. It works by blocking a certain natural substance (histamine) that causes allergic symptoms. Do not use this medication to treat red or irritated eyes due to wearing contact lenses. Contact your doctor for further instructions if this occurs.
11-Digit NDC Billing Format:
70069071101
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:
Somerset Therapeutics, Llc
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):
BEPOTASTINE BESILATE 15 mg/mL
Pharmacologic Class(es):
Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
Sample Package:
No
FDA Application Number:
ANDA217770
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-10-2024
Listing Expiration Date:
12-31-2025
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 70069-711-01?

The NDC Packaged Code 70069-711-01 is assigned to a package of 1 bottle in 1 carton / 5 ml in 1 bottle of Bepotastine Besilate, a human prescription drug labeled by Somerset Therapeutics, Llc. The product's dosage form is solution and is administered via ophthalmic form.

Is NDC 70069-711 included in the NDC Directory?

Yes, Bepotastine Besilate with product code 70069-711 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on October 10, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70069-711-01?

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 70069-711-01?

The 11-digit format is 70069071101. 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
5-3-270069-711-015-4-270069-0711-01