Azithromycin Tablet, Film Coated
Product Images NDC 68180-862

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Azithromycin (NDC 68180-862). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

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Structure (1ede87c9 811c 4887 A274 A248a1e58a9d 01)

Chemical structure of azithromycin, a macrolide antibiotic consisting of a complex lactone ring with attached sugar moieties and various functional groups, as shown in the diagram.*

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Image (1ede87c9 811c 4887 A274 A248a1e58a9d 02)

Instructional diagrams showing how to remove azithromycin tablets from blister packs for the 250 mg and 500 mg film-coated oral tablets. Steps include tearing along perforations, peeling paper to expose the foil, and pushing the tablet through the foil for each strength.*

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Bottle Label (30 Tablets)

Azithromycin Tablets USP 250 mg film-coated oral tablets label by Lupin Pharmaceuticals, Inc. The label states 30 tablets per container and includes the NDC code 68180-861-06. Storage and dosage instructions are present, along with manufacturing information for Lupin Pharmaceuticals in the US and Lupin Limited in India. The label also warns pharmacists to dispense with a patient information leaflet.*

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Carton (250 mg)

The image shows the packaging label for Azithromycin Tablets USP 250 mg film-coated tablets, manufactured by Lupin Pharmaceuticals, Inc. The label indicates that the product is prescription only and contains 3 cartons each with 6 tablets, totaling 18 tablets. The label includes storage instructions, manufacturer details, and administration directions referencing a full course of antibiotic therapy in 5 daily doses.*

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250 mg (1ede87c9 811c 4887 A274 A248a1e58a9d 05)

Azithromycin Tablets USP 250 mg film-coated oral tablets packaging label from Lupin Pharmaceuticals, Inc. The label indicates a 6-tablet count and mentions the product is for prescription use with directions for a full course in 5 daily doses. The label includes the NDC 68180-861-11 and features a white, green, and light purple color scheme.*

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Blister Card (250 mg)

Packaging label for azithromycin 250 mg tablets by Lupin Pharmaceuticals, Inc. The label includes dosing instructions for a 5-day oral course, with daily tablet counts clearly stated. Multiple similar panels are arranged in a grid, each containing dosage and manufacturer information, barcodes, and lot details.*

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Bottle Label (30 tablets)

Azithromycin Tablets USP 500 mg film-coated tablets label. The carton holds 30 tablets and is manufactured by Lupin Pharmaceuticals, Inc. The label advises dispensing with a patient information leaflet and indicates Rx only. Storage instructions and manufacturer details are also included.*

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Carton (500 mg)

Azithromycin Tablets USP 500 mg film-coated tablets carton packaging from Lupin Pharmaceuticals, Inc. The label includes directions for use, an NDC number, and indicates a package containing 2 cartons with 3 tablets each. The label is designed for oral use and specifies Rx only.*

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500 mg (1ede87c9 811c 4887 A274 A248a1e58a9d 09)

Azithromycin Tablets USP 500 mg film-coated tablets packaging label by Lupin Pharmaceuticals, Inc. The carton displays 3 tablets with dosage information and handling instructions. The label shows the NDC code 68180-862-11 and manufacturer details.*

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Blister Card (500 mg)

Packaging label for azithromycin film-coated tablets by Lupin Pharmaceuticals, Inc. The label layout includes multiple barcode panels and data matrices, intended for blister packaging. The label accommodates azithromycin tablets with strengths of 250 mg and 500 mg, oral route.*

* 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.