Zithromax Tablet, Film Coated
Product Images NDC 67296-0020

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Zithromax (NDC 67296-0020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Chemical Structure (Zithromax 01)

FDA Label Image

Logo (Zithromax 02)

Logo (Zithromax 02)
This text indicates that the product is distributed by Pfizer Labs, which is a division of Pfizer Inc based in New York City with the zip code 10017.*
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Logo (Zithromax 02a)

Logo (Zithromax 02a)
This text mentions that the product is being distributed by Pfizer Labs, a division of Pfizer Inc located in NY, NY 10017.*
FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
This is a description for Zithromax® (azithromycin) tablets. Each tablet contains azithromycin dihydrate equivalent to 250 mg of azithromycin. It is required to store between 15° to 30°C (59° to 86°F) and be dispensed in tight, child-resistant containers. The NDC number is 0069-3060-30 and it is distributed by Pfizer Labs, Division of Pfizer Inc, NY, NY 10017. The tablets are available in packs of 30 and are for prescription use only.*
FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
The text provides instructions for taking Zithromax (azithromycin) for a full course of antibiotics. It advises taking 2 tablets on the first day and then 1 tablet daily for the next 4 days. Zithromax is claimed to keep working within Days 6-10. The text also mentions the cost-effectiveness of Zithromax compared to other antibiotics.*
FDA Label Image

Principal Display Panel (250 mg)

FDA Label Image

Principal Display Panel (250 mg)

FDA Label Image

Principal Display Panel (250 mg Tablet Blister Pack Box)

Principal Display Panel (250 mg Tablet Blister Pack Box)
This text appears to be an advertisement for Zithromax® (azithromycin) tablets in unit dose packaging. It mentions that the tablets are for information use only and a pack contains 50 tablets. The product is described as equivalent to 50mg of azithromycin. The information also includes a contact address for further inquiries.*
FDA Label Image

Principal Display Panel (500 mg)

Principal Display Panel (500 mg)
This text provides dosage and usage information for Zithromax tablets containing azithromycin. It mentions storing the tablets between 15 to 30 degrees Celsius (59 to 86 degrees Fahrenheit) and dispensing in a tight container. The tablets are distributed by Pfizer Labs and made in Singapore, with each tablet containing 500 mg of azithromycin. The text also includes the product code, expiration date, and GTIN information.*
FDA Label Image

Principal Display Panel (500 mg)

Principal Display Panel (500 mg)
Zithromax is an oral antibiotic that is taken once a day for 3 days. The medication is available in 500mg tablets and comes in a pack of 3 tablets. It is important to finish the full course of treatment to prevent the infection from returning. Common side effects may include diarrhea, nausea, and stomach pain. Allergic reactions are rare but should be reported to a healthcare provider immediately. If you have any questions or concerns about Zithromax, it is recommended to consult with your healthcare provider.*
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Principal Display Panel (500 mg)

FDA Label Image

Principal Display Panel (300 mg Bottle Label)

Principal Display Panel (300 mg Bottle Label)
This is a set of instructions for the oral use of a medication called Zithromax (azithromycin). The text includes information on storage conditions, dosage, and mixing directions. It specifies that the medication is to be kept below 30°C, must be protected from freezing, and should be used within 10 days after mixing with water. The medication is cherry flavored and contains 300 mg of azithromycin per dose.*
FDA Label Image

Principal Display Panel (300 mg Bottle Carton)

Principal Display Panel (300 mg Bottle Carton)
This is a label for Zithromax (azithromycin) oral suspension, providing information on dosage, storage instructions, and the flavor. It also includes the caution "SHAKE WELL BEFORE USING." The label indicates that an oversized bottle provides an extra 300 mg when mixed and reiterates the dosages for different purposes. It further specifies that the product is for oral use only and must be stored below 30°C.*
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Principal Display Panel (600 mg Bottle Label)

Principal Display Panel (600 mg Bottle Label)
This text provides instructions for the oral use of a medication called Zithromax (azithromycin). It includes details on dosage, mixing directions, storage conditions, and the cherry flavor of the oral suspension. Users are advised to store the dry powder below 30°C, protect it from freezing, mix it with water before use, and shake well before using. The medication is available in a bottle that provides extra space for shaking, and it contains 200 mg per 5 mL. Once the dosage is complete, the bottle should be discarded.*
FDA Label Image

Principal Display Panel (600 mg Bottle Carton)

Principal Display Panel (600 mg Bottle Carton)
This is a medication label for Zithromax (azithromycin) oral suspension. The product contains 600 mg of azithromycin and is to be stored below 30°C. The dosage is 200 mg per 5 mL of suspension, and it is cherry flavored. The label instructs to shake well before use and includes prescribing information. It warns to protect from freezing and includes the manufacturer's address as well.*
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Principal Display Panel (900 mg Bottle Label)

Principal Display Panel (900 mg Bottle Label)
This text provides information on Zithromax (azithromycin) for oral suspension in cherry flavor. It includes storage instructions, dosage and use details, mixing directions, and expiration guidelines. The text also mentions the quantity of powder and water needed for preparation, along with an oversized bottle for shaking. Additionally, there is a unique identifier number (NDC), the amount of azithromycin when mixed, and the manufacturer's details for Labs, a division of Pfizer Inc.*
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Principal Display Panel (900 mg Bottle Carton)

Principal Display Panel (900 mg Bottle Carton)
This text appears to be detailing information about a medication called Zithromax (azithromycin) for oral suspension. It includes instructions on dosage, usage, storage, and important warnings such as shaking well before use and protecting from freezing. The medication contains 900 mg of active ingredient and has a cherry flavor. The text suggests that each teaspoonful contains a certain amount of the active ingredient and that it should be used within 10 days after mixing. It also provides contact information for inquiries.*
FDA Label Image

Principal Display Panel (1200 mg Bottle Label)

Principal Display Panel (1200 mg Bottle Label)
This text provides dosing and usage instructions for Zithromax (azithromycin) oral suspension, emphasizing proper storage and mixing. It includes details such as protecting the powder from freezing, mixing directions, storage guidelines, and discarding unused suspension after 10 days. The medication is cherry-flavored and contains 1200 mg of azithromycin. The product is distributed by Pfizer Labs.*
FDA Label Image

Principal Display Panel (1200 mg Bottle Carton)

Principal Display Panel (1200 mg Bottle Carton)
This text provides information about an oral suspension medication named Zithromax (azithromycin) with a cherry flavor, containing 1200 mg per dosage. It includes usage instructions, warnings against freezing, dosage details, and the address of the distributor. The medication is intended for oral use only, and it is important to shake well before using.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.