Azithromycin Tablet, Film Coated
Product Images NDC 65862-642

7 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Azithromycin (NDC 65862-642). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (250 mg (30 Tablets Bottle))

Package Label-principal Display Panel (250 mg (30 Tablets Bottle))
Azithromycin Tablets USP 250 mg film-coated tablet label. The label states the active ingredient is azithromycin dihydrate equivalent to 250 mg azithromycin. The package contains 30 tablets and is labeled for prescription use only. It is distributed by Aurobindo Pharma USA, Inc. and made in India. Storage instructions and dispensing details are also included.*
FDA Label Image

Package Label-principal Display Panel (250 mg (1 x 6) Unit-dose Tablets)

Package Label-principal Display Panel (250 mg (1 x 6) Unit-dose Tablets)
Packaging label for Azithromycin Tablets, USP 250 mg film-coated tablets by Aurobindo Pharma Limited. The label indicates a package containing 6 tablets (1 blister of six 250 mg tablets) for a full course of antibiotic therapy in 5 daily doses. The label includes dosage instructions, storage information, side effects, and prescribing information references. Distributed by Aurobindo Pharma USA, Inc.*
FDA Label Image

Package Label-principal Display Panel (250 mg (3 x 6) Unit-dose Tablets)

Package Label-principal Display Panel (250 mg (3 x 6) Unit-dose Tablets)
Azithromycin Tablets, USP 250 mg film-coated tablets packaging label. The label is from Aurobindo Pharma Limited, showing Rx only, with a full course in 5 daily doses. The package contains 18 tablets (3 cartons of 6 tablets each). Storage and dosage instructions are partially visible. Distributed by Aurobindo Pharma USA, Inc., made in India.*
FDA Label Image

Package Label-principal Display Panel (500 mg (30 Tablets Bottle))

Package Label-principal Display Panel (500 mg (30 Tablets Bottle))
Azithromycin Tablets USP 500 mg film-coated tablets packaging label. The label shows the product name, strength, and dosage form, with a quantity of 30 tablets. It is labeled for prescription use only and distributed by Aurobindo Pharma USA, Inc., with manufacturing in India by Aurobindo Pharma Limited. The label includes storage instructions and a barcode.*
FDA Label Image

Package Label-principal Display Panel (500 mg 3 Tablets (1 Card x Three 500 mg Tablets))

Package Label-principal Display Panel (500 mg 3 Tablets (1 Card x Three 500 mg Tablets))
Packaging label for Azithromycin Tablets, USP 500 mg by Aurobindo Pharma Limited. The label states Rx only and indicates a package size of 3 tablets (1 blister containing three 500 mg tablets). Distribution is by Aurobindo Pharma USA, Inc., with a barcode and NDC 65862-642-64 visible. The label includes dosage instructions and storage information.*
FDA Label Image

Package Label-principal Display Panel (500 mg 9 Tablets (3 Cards x Three 500 mg Tablets))

Package Label-principal Display Panel (500 mg 9 Tablets (3 Cards x Three 500 mg Tablets))
Azithromycin Tablets, USP 500 mg film-coated tablets carton by Aurobindo Pharma Limited. The package contains 9 tablets (3 cartons x 3 tablets each) and is labeled for prescription use only. Storage instructions and prescribing information references are provided. Distributed by Aurobindo Pharma USA, Inc., made in India.*
FDA Label Image

Chemical Structure (Azithromycin Str)

Chemical Structure (Azithromycin Str)
Chemical structure diagram of azithromycin, showing its complex macrolide ring system with various attached functional groups including methyl, hydroxyl, and nitrogen-containing moieties.*

* 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.