NDC Package 72266-158-01 Moxifloxacin Ophthalmic Solution

Moxifloxacin Ophthalmic 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:
72266-158-01
Package Description:
1 BOTTLE in 1 CARTON / 3 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Moxifloxacin Ophthalmic Solution
Non-Proprietary Name:
Moxifloxacin Ophthalmic
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 influenzae Haemophilus parainfluenzae* Chlamydia trachomatis *Efficacy for this organism was studied in fewer than 10 infections.
11-Digit NDC Billing Format:
72266015801
NDC to RxNorm Crosswalk:
  • RxCUI: 403818 - moxifloxacin HCl 0.5 % Ophthalmic Solution
  • RxCUI: 403818 - moxifloxacin 5 MG/ML Ophthalmic Solution
  • RxCUI: 403818 - moxifloxacin (as moxifloxacin HCl) 0.5 % Ophthalmic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fosun Pharma Usa Inc.
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    FDA Application Number:
    ANDA208778
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-24-2020
    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 72266-158-01?

    The NDC Packaged Code 72266-158-01 is assigned to a package of 1 bottle in 1 carton / 3 ml in 1 bottle of Moxifloxacin Ophthalmic Solution, a human prescription drug labeled by Fosun Pharma Usa Inc.. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 72266-158 included in the NDC Directory?

    Yes, Moxifloxacin Ophthalmic Solution with product code 72266-158 is active and included in the NDC Directory. The product was first marketed by Fosun Pharma Usa Inc. on August 24, 2020 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 11-digit format for NDC 72266-158-01?

    The 11-digit format is 72266015801. 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
    5-3-272266-158-015-4-272266-0158-01