Azithromycin Dihydrate Powder, For Suspension
Product Images NDC 70436-221

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azithromycin Dihydrate (NDC 70436-221). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Slate Run Pharmaceuticals, 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

Azithromycin Chem Structure (Image 01)

Azithromycin Chem Structure (Image 01)
Chemical structure of azithromycin dihydrate, depicting the molecular arrangement of atoms and bonds characteristic of this antibiotic compound.*
FDA Label Image

300 mg Bottle Label (Image 02)

300 mg Bottle Label (Image 02)
Azithromycin for Oral Suspension USP 100 mg per 5 mL powder for suspension label. Contains 300 mg azithromycin (15 mL when mixed). Manufactured by Zhejiang Poly Pharm and distributed by Slate Run Pharmaceuticals, LLC. Includes mixing directions, storage instructions, and child-resistant packaging information.*
FDA Label Image

600 mg Bottle Label (Image 03)

600 mg Bottle Label (Image 03)
Label for azithromycin dihydrate oral suspension USP, 200 mg per 5 mL strength, powder for suspension form. The label states the total active ingredient is 600 mg per 15 mL of mixed suspension. It includes dosage and mixing directions, manufacturer Zhejiang Poly Pharm Co., Ltd., and distributor Slate Run Pharmaceuticals, LLC. The label also mentions child-resistant packaging, storage conditions, and an NDC number 70436-221-34.*
FDA Label Image

1200 mg Bottle Label (Image 04)

1200 mg Bottle Label (Image 04)
Label for Azithromycin for Oral Suspension USP powder for suspension, showing 200 mg per 5 mL strength. The label includes dosage form as oral suspension, instructions for mixing 15 mL of water, storage conditions, and manufacturer Zhejiang Poly Pharm Co., Ltd. Distributed by Slate Run Pharmaceuticals, LLC. It specifies child-resistant packaging and dosing 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.