NDC Package 43063-715-02 Azithromycin Monohydrate

Tablet 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:
43063-715-02
Package Description:
2 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Azithromycin Monohydrate
Non-Proprietary Name:
Azithromycin Monohydrate
Substance 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:
43063071502
NDC to RxNorm Crosswalk:
  • RxCUI: 248656 - azithromycin 500 MG Oral Tablet
  • RxCUI: 248656 - azithromycin 500 MG (as azithromycin monohydrate) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Pd-rx Pharmaceuticals, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA065399
    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
    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.

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    Frequently Asked Questions

    What is NDC 43063-715-02?

    The NDC Packaged Code 43063-715-02 is assigned to a package of 2 tablet in 1 bottle, plastic of Azithromycin Monohydrate, a human prescription drug labeled by Pd-rx Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 43063-715 included in the NDC Directory?

    Yes, Azithromycin Monohydrate with product code 43063-715 is active and included in the NDC Directory. The product was first marketed by Pd-rx Pharmaceuticals, Inc. on August 18, 2015.

    What is the 11-digit format for NDC 43063-715-02?

    The 11-digit format is 43063071502. 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
    5-3-243063-715-025-4-243063-0715-02