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  5. NDC Package Code: 70069-081-01 Moxifloxacin Hydrochloride

NDC Package 70069-081-01 Moxifloxacin Hydrochloride

Solution/ Drops 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:
70069-081-01
Package Description:
1 BOTTLE in 1 CARTON / 3 mL in 1 BOTTLE
Product Code:
70069-081
Proprietary Name:
Moxifloxacin Hydrochloride
Non-Proprietary Name:
Moxifloxacin Hydrochloride
Substance Name:
Moxifloxacin Hydrochloride
Usage Information:
Moxifloxacin ophthalmic solution is indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms:Corynebacterium species* Micrococcus luteus* Staphylococcus aureus Staphylococcus epidermidis Staphylococcus haemolyticus Staphylococcus hominis Staphylococcus warneri* Streptococcus pneumoniae Streptococcus viridans group Acinetobacter lwoffii* Haemophilus influenza Haemophilus parainfluenzae* Chlamydia trachomatis*Efficacy for this organism was studied in fewer than 10 infections.
11-Digit NDC Billing Format:
70069008101
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/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s):
Ophthalmic - Administration to the external eye.
Active Ingredient(s):
MOXIFLOXACIN HYDROCHLORIDE 5 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA209698
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-25-2024
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 70069-081-01?

The NDC Packaged Code 70069-081-01 is assigned to a package of 1 bottle in 1 carton / 3 ml in 1 bottle of Moxifloxacin Hydrochloride, 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 70069-081 included in the NDC Directory?

Yes, Moxifloxacin Hydrochloride with product code 70069-081 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on November 25, 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 70069-081-01?

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 70069-081-01?

The 11-digit format is 70069008101. 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
5-3-270069-081-015-4-270069-0081-01