NDC 61919-776 Zithromax

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
61919-776
Proprietary Name:
Zithromax
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Direct Rx
Labeler Code:
61919
Start Marketing Date: [9]
05-27-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
E
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE (WHITE FILM-COATED))
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
W964

Product Packages

NDC Code 61919-776-02

Package Description: 2 TABLET, FILM COATED in 1 BOTTLE

NDC Code 61919-776-03

Package Description: 3 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 61919-776?

The NDC code 61919-776 is assigned by the FDA to the product Zithromax which is product labeled by Direct Rx. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61919-776-02 2 tablet, film coated in 1 bottle , 61919-776-03 3 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Zithromax?

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.

Which are Zithromax UNII Codes?

The UNII codes for the active ingredients in this product are:

  • AZITHROMYCIN ANHYDROUS (UNII: J2KLZ20U1M)
  • AZITHROMYCIN ANHYDROUS (UNII: J2KLZ20U1M) (Active Moiety)

Which are Zithromax Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Zithromax?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".