Erythromycin Ethylsuccinate Granule, For Suspension
Product Images NDC 62559-631

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Erythromycin Ethylsuccinate (NDC 62559-631). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani 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.

FDA Label Image

200mg-5ml_label (200mg 5ml Label)

This text describes the preparation and dosage of Erythromycin ethylsuccinate for oral suspension. The granules must be stored below 86°F (30°C) and when prepared as directed, each 5 mL teaspoonful contains erythromycin ethylsuccinate 2 for Oral Suspension USP equivalent to 200 mg of erythromycin in a cherry-flavored suspension. Its usual dose for children is 30 to 50 mg/kg/day in divided doses. The manufacturer is ANI Pharmaceuticals, Inc. and it is important to see the package insert for adult dose and full prescribing information.*

FDA Label Image

400mg-5ml_label (400mg 5ml Label)

This is a description of a medication called Erythromycin ethylsuccinate oral suspension. The medication comes in granule form and should be stored below 86°F (30°C) before mixing with 50 mL of water. Once added, the solution should be shaken vigorously to make 100 mL of a cherry-flavored suspension that contains 400 mg of Erythromycin ethylsuccinate per 5 mL (teaspoonful). The reconstituted suspension does not require refrigeration and can be taken on an empty stomach. The usual dose for children is 30 to 50 mg/kg/day in divided doses. The medication should be stored below 77°F (25°C) and used within 35 days after mixing.*

FDA Label Image

Ani-logo (Ani Logo)

FDA Label Image

Structure (Structure)

* 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.