Azithromycin Dihydrate
Product Images NDC 70882-107

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Azithromycin Dihydrate (NDC 70882-107). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cambridge Therapeutics Technologies, Llc, 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

Structure (Azithromycin Tablets Usp Apotex 1)

Structure (Azithromycin Tablets Usp   Apotex 1)
Chemical structure of azithromycin dihydrate, depicting its macrolide ring with attached sugar moieties and various functional groups.*
FDA Label Image

Azithromycin Tablets, Usp 250 mg (Azithromycin Tablets Usp Apotex 2)

Azithromycin Tablets, Usp 250 mg (Azithromycin Tablets Usp   Apotex 2)
Azithromycin Tablets, USP 250 mg carton label showing a unit of use containing 6 tablets. The label includes the proprietary name in purple text, dosage strength, and manufacturer and distributor information from Apotex Inc. and Cambridge Therapeutic Technologies, LLC. The label also features a pill image marked APO AZZ50 and a barcode.*
FDA Label Image

Azithromycin Tablets, Usp 500 mg (Azithromycin Tablets Usp Apotex 3)

Azithromycin Tablets, Usp 500 mg (Azithromycin Tablets Usp   Apotex 3)
Packaging label for Azithromycin Tablets, USP 500 mg from Cambridge Therapeutic Technologies. The label highlights a full course of antibiotic therapy in 3 daily doses, with a unit of use containing 3 tablets of 500 mg each. The label includes standard warnings, NDC 70882-118-03, and the Cambridge Therapeutic Technologies logo and address.*

* 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.