Erythromycin Ethylsuccinate Suspension
Product Images NDC 69238-1503

3 FDA label images from Amneal Pharmaceuticals Ny Llc · 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 Erythromycin Ethylsuccinate (NDC 69238-1503). 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

Formula Structure (Erythromycin Ethylsuccinate For Oral Suspension Us 1)

Formula Structure (Erythromycin Ethylsuccinate For Oral Suspension Us 1)
Chemical structure of erythromycin, the active ingredient in Erythromycin Ethylsuccinate oral suspension products.*
FDA Label Image

200 mg Label (Erythromycin Ethylsuccinate For Oral Suspension Us 2)

200 mg Label (Erythromycin Ethylsuccinate For Oral Suspension Us 2)
Label for Erythromycin Ethylsuccinate oral suspension, USP, 200 mg/5 mL strength by Amneal Pharmaceuticals NY LLC. The 100 mL bottle label shows directions for mixing and dosage details, emphasizing 200 mg erythromycin activity per 5 mL when reconstituted. The label includes storage instructions and a barcode.*
FDA Label Image

400 mg Label (Erythromycin Ethylsuccinate For Oral Suspension Us 3)

400 mg Label (Erythromycin Ethylsuccinate For Oral Suspension Us 3)
Label for Erythromycin Ethylsuccinate for Oral Suspension, USP 400 mg/5 mL, an oral suspension by Amneal Pharmaceuticals NY LLC. The label includes dosing instructions, mixing directions with water, storage conditions, and warnings. It states the erythromycin activity per 5 mL when reconstituted and includes a barcode and lot/expiration date area.*

* 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.