Erythromycin Ethylsuccinate Suspension
Product Images NDC 60219-1503

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Erythromycin Ethylsuccinate (NDC 60219-1503). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

1 (Erythromycin Ethylsuccinate For Oral Suspension Us 1)

1 (Erythromycin Ethylsuccinate For Oral Suspension Us 1)
Chemical structure of erythromycin, the active ingredient in erythromycin ethylsuccinate oral suspension by Amneal Pharmaceuticals NY LLC.*
FDA Label Image

1 (Erythromycin Ethylsuccinate For Oral Suspension Us 2)

1 (Erythromycin Ethylsuccinate For Oral Suspension Us 2)
Label for Erythromycin Ethylsuccinate oral suspension, USP 200 mg/5 mL by Amneal Pharmaceuticals NY LLC. The label includes preparation directions, dosage, storage instructions, and manufacturer/distributor details. It specifies the dosage form as a fruit-flavored aqueous suspension, requires mixing with water, is for prescription use only, and provides handling instructions for storage and usage.*
FDA Label Image

2 (Erythromycin Ethylsuccinate For Oral Suspension Us 3)

2 (Erythromycin Ethylsuccinate For Oral Suspension Us 3)
Label for Erythromycin Ethylsuccinate for Oral Suspension, USP, 400 mg/5 mL strength. This 100 mL oral suspension is manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. The label includes directions for mixing, storage instructions, and dosage information, with a banana flavor mentioned.*

* 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.