NDC Package 71205-119-03 Azithromycin Monohydrate

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
71205-119-03
Package Description:
3 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Azithromycin Monohydrate
Usage Information:
•Acute bacterial exacerbations of chronic bronchitis due to Haemophilus influenzae , Moraxella catarrhalis, or Streptococcus pneumoniae .•Acute bacterial sinusitis due to Haemophilus influenzae , Moraxella catarrhalis or Streptococcus pneumoniae .•Community-acquired pneumonia due to Chlamydophila pneumoniae , Haemophilus influenzae , Mycoplasma pneumoniae, or Streptococcus pneumoniae in patients appropriate for oral therapy.•Pharyngitis/tonsillitis caused by Streptococcus pyogenes as an alternative to first-line therapy in individuals who cannot use first-line therapy.•Uncomplicated skin and skin structure infections due to Staphylococcus aureus , Streptococcus pyogenes , or Streptococcus agalactiae .•Urethritis and cervicitis due to Chlamydia trachomatis or Neisseria gonorrhoeae .•Genital ulcer disease in men due to Haemophilus ducreyi (chancroid). Due to the small number of women included in clinical trials, the efficacy of azithromycin in the treatment of chancroid in women has not been established.
11-Digit NDC Billing Format:
71205011903
Labeler Name:
Proficient Rx Lp
Sample Package:
No
FDA Application Number:
ANDA065398
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-18-2015
End Marketing Date:
07-31-2024
Listing Expiration Date:
07-31-2024
Exclude Flag:
D
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
71205-119-044 TABLET in 1 BOTTLE
71205-119-066 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71205-119-03?

The NDC Packaged Code 71205-119-03 is assigned to a package of 3 tablet in 1 bottle of Azithromycin Monohydrate, labeled by Proficient Rx Lp. The product's dosage form is and is administered via form.

Is NDC 71205-119 included in the NDC Directory?

No, Azithromycin Monohydrate with product code 71205-119 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Proficient Rx Lp on August 18, 2015 and its listing in the NDC Directory is set to expire on July 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71205-119-03?

The 11-digit format is 71205011903. 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
5-3-271205-119-035-4-271205-0119-03