NDC Package 0069-3110-19 Zithromax

Azithromycin Dihydrate Powder, For Suspension Oral - 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:
0069-3110-19
Package Description:
1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Zithromax
Non-Proprietary Name:
Azithromycin Dihydrate
Substance Name:
Azithromycin Dihydrate
Usage Information:
Azithromycin is used to treat a wide variety of bacterial infections. It is a macrolide-type antibiotic. It works by stopping the growth of bacteria. This medication will not work for viral infections (such as common cold, flu). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.
11-Digit NDC Billing Format:
00069311019
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 105260 - Zithromax 200 MG in 5 mL Oral Suspension
  • RxCUI: 105260 - azithromycin 40 MG/ML Oral Suspension [Zithromax]
  • RxCUI: 105260 - Zithromax 200 MG per 5 ML Oral Suspension
  • RxCUI: 105260 - Zithromax 40 MG/ML Oral Suspension
  • RxCUI: 141963 - azithromycin 200 MG in 5 mL Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Pfizer Laboratories Div Pfizer Inc
    Dosage Form:
    Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA050710
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-19-1995
    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 0069-3110-19?

    The NDC Packaged Code 0069-3110-19 is assigned to a package of 1 bottle in 1 carton / 15 ml in 1 bottle of Zithromax, a human prescription drug labeled by Pfizer Laboratories Div Pfizer Inc. The product's dosage form is powder, for suspension and is administered via oral form.

    Is NDC 0069-3110 included in the NDC Directory?

    Yes, Zithromax with product code 0069-3110 is active and included in the NDC Directory. The product was first marketed by Pfizer Laboratories Div Pfizer Inc on October 19, 1995 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 0069-3110-19?

    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 0069-3110-19?

    The 11-digit format is 00069311019. 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 4-4-2 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
    4-4-20069-3110-195-4-200069-3110-19