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)

Chemical Structure (Zithromax 01)
Chemical structure diagram of azithromycin dihydrate showing the detailed molecular configuration with labeled chemical groups and bonds.*
FDA Label Image

Logo (Zithromax 02)

FDA Label Image

Logo (Zithromax 02a)

FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
Zithromax 250 mg film-coated tablets label by Pfizer Labs. The label specifies azithromycin tablets, a prescription medication, with a quantity of 30 tablets. It includes storage instructions, dosage notes, and a barcode. The label emphasizes dispensing in child-resistant containers and displays the Pfizer logo.*
FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
The image shows a Zithromax 250 mg film-coated tablet carton label by Redpharm Drug. This oral antibiotic package contains 6 tablets marketed as Z-Pak, a 5-day antibiotic therapy with a dosing guide illustrated for taking 2 tablets on the first day and 1 tablet daily for the next 4 days. The label highlights cost benefits and usage instructions.*
FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
This image shows multiple blister card labels for Zithromax 250 mg tablets. Each label states the product name Zithromax with the generic name azithromycin, strength 250 mg, and dosage form tablet. The labels indicate distribution by Pfizer Labs, a division of Pfizer Inc, NY, and that the product is made in the USA. Additional label areas include placeholders for expiration and lot numbers, along with regulatory codes.*
FDA Label Image

Principal Display Panel (250 mg)

Principal Display Panel (250 mg)
Packaging label for Zithromax (azithromycin dihydrate) tablets, film coated, 250 mg strength by Redpharm Drug. The label includes branding for Z-Pak and indicates a 5-day antibiotic therapy course with 3 cards of 6 tablets. The background is teal with white and yellow text and a prominent purple and yellow 'Z' logo on the front panel.*
FDA Label Image

Principal Display Panel (250 mg Tablet Blister Pack Box)

Principal Display Panel (250 mg Tablet Blister Pack Box)
Packaging label for Zithromax (azithromycin) tablets, 250 mg strength, film-coated oral tablets. The label shows the Pfizer logo and states the product is for in-institution use only with a package count of 50 tablets. It includes storage instructions and dosage information, and notes distribution by Pfizer Labs, NY, NY 10017.*
FDA Label Image

Principal Display Panel (500 mg)

Principal Display Panel (500 mg)
Zithromax 500 mg tablets packaging label showing azithromycin as the active ingredient. The label includes dosage information, storage instructions, and manufacturer details including Pfizer Labs. The package contains 30 film-coated oral tablets. Product NDC on the label is 0069-3070-30.*
FDA Label Image

Principal Display Panel (500 mg)

Principal Display Panel (500 mg)
Bottle and carton labeling for Zithromax (azithromycin) 500 mg tablets, oral film-coated tablets in a 3-tablet pack known as TRI-PAK. Labeler is Redpharm Drug. The packaging highlights a 3-day course with instructions and side effects information. The label features the Zithromax logo, dosage instructions, and a dosage schedule illustration.*
FDA Label Image

Principal Display Panel (500 mg)

Principal Display Panel (500 mg)
Packaging label for Zithromax TRI-PAK 500 mg tablets (azithromycin), consisting of three cards each containing three 500 mg tablets. The carton is predominantly yellow and white with the brand name and dosage prominently displayed. The label shows it is labeled by Pfizer Labs, a division of Pfizer Inc, and includes storage instructions, dosage information reference, and barcodes. The label notes the tablets contain azithromycin dihydrate equivalent to 500 mg azithromycin and specifies storage between 15° to 30°C.*
FDA Label Image

Principal Display Panel (300 mg Bottle Label)

Principal Display Panel (300 mg Bottle Label)
Zithromax oral suspension label for azithromycin, showing 100 mg per 5 mL strength in cherry flavor. The label includes dosing instructions, storage conditions, and a 300 mg total azithromycin content when mixed to 15 mL. Distributed by Pfizer, the label features the Pfizer logo and cautions for oral use only.*
FDA Label Image

Principal Display Panel (300 mg Bottle Carton)

Principal Display Panel (300 mg Bottle Carton)
Zithromax oral suspension label with azithromycin 100 mg per 5 mL strength, cherry flavored. The label highlights a 300 mg (15 mL when mixed) dosage, distributed by Pfizer Labs. The packaging instructs to shake well before using and store suspension at 5° to 30°C (41° to 86°F). This is for oral use only and is a prescription drug product.*
FDA Label Image

Principal Display Panel (600 mg Bottle Label)

Principal Display Panel (600 mg Bottle Label)
Zithromax (azithromycin) oral suspension label showing 200 mg per 5 mL strength in a cherry-flavored formulation. The label includes mixing directions for 600 mg total content, storage instructions, and warnings. The labeler is Pfizer Labs, a division of Pfizer Inc.*
FDA Label Image

Principal Display Panel (600 mg Bottle Carton)

Principal Display Panel (600 mg Bottle Carton)
Packaging label for Zithromax oral suspension, 200 mg per 5 mL strength. The label shows it is azithromycin-based, cherry flavored, and for oral use only. The product is distributed by Pfizer Labs. The label includes directions to shake well before use, storage guidelines, and dosage information. The NDC on the label is 0069-3120-19.*
FDA Label Image

Principal Display Panel (900 mg Bottle Label)

Principal Display Panel (900 mg Bottle Label)
Zithromax oral suspension label showing azithromycin for oral use only, 200 mg per 5 mL strength, cherry flavored, with a total of 900 mg azithromycin in the bottle. The label includes Pfizer branding, storage instructions, mixing directions, and usage warnings. It is labeled for prescription use only.*
FDA Label Image

Principal Display Panel (900 mg Bottle Carton)

Principal Display Panel (900 mg Bottle Carton)
Packaging label for Zithromax (azithromycin) oral suspension, 200 mg per 5 mL, 900 mg (22.5 mL when mixed), cherry flavored. The label indicates it is for oral use only and displays the Pfizer logo. Includes storage instructions and dosage information with barcode and NDC 0069-3130-19.*
FDA Label Image

Principal Display Panel (1200 mg Bottle Label)

Principal Display Panel (1200 mg Bottle Label)
Zithromax azithromycin oral suspension label by Pfizer, 200 mg per 5 mL strength, cherry flavored. The label provides preparation and usage instructions for the 1200 mg total azithromycin content when mixed to 30 mL. It includes storage directions, dosage caution, and a barcode. The labeler is Pfizer Inc.*
FDA Label Image

Principal Display Panel (1200 mg Bottle Carton)

Principal Display Panel (1200 mg Bottle Carton)
Packaging label for Zithromax oral suspension by Pfizer, containing azithromycin. The label indicates a strength of 200 mg per 5 mL after mixing, with a total of 1200 mg in 30 mL when mixed. The product is cherry flavored and for oral use only. The label includes storage instructions and dosage guidance.*

* 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.