Azithromycin Tablet, Film Coated
Product Images NDC 72189-093

4 FDA label images from Direct Rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azithromycin (NDC 72189-093). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

72189 0089 06

72189 0089 06
AZITHROMYCIN 250 mg oral film-coated tablets carton label shows 6 tablets per package. The label indicates azithromycin as the active ingredient, with each tablet containing 250 mg of azithromycin dihydrate equivalent. The product is generic for Zithromax and is labeled by Direct Rx. Lot number and packaging details are also visible.*
FDA Label Image

72189 087 10

72189 087 10
AZITHROMYCIN 250 mg film coated tablets in a package of 10 tablets. The label shows the generic name ZITHROMAX and states each tablet contains Azithromycin dihydrate USP equivalent to 250 mg azithromycin. Manufacturer and distributor is DIRECT RX. The label includes lot number, expiration date, and NDC codes.*
FDA Label Image

72189 088 03

72189 088 03
Label for Azithromycin 500 mg film-coated tablets by Direct Rx. The package contains 3 tablets. It is a generic product equivalent to Zithromax, with each tablet containing azithromycin dihydrate USP equivalent to 500 mg azithromycin. The label includes lot number, expiration date, packaging and distribution information.*
FDA Label Image

093 (72189 093 06)

093 (72189 093 06)
AZITHROMYCIN 250 mg film-coated tablets packaging label showing a quantity of 6 tablets. The label indicates the product is a generic for ZITHROMAX and contains azithromycin dihydrate USP equivalent to 250 mg azithromycin per tablet. The label also identifies the labeler as DIRECT RX with lot number 06AP2008 and discard date 3/31/21.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.