Erythromycin Ethylsuccinate Suspension
Product Images NDC 52536-132

3 FDA label images from Wilshire Pharmaceuticals · 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 52536-132). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wilshire Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Erythromycin 01)

Chemical Structure (Erythromycin 01)
Chemical structure of meclizine hydrochloride, showing its molecular formula with multiple rings, hydroxyl groups, and functional groups indicated by lines and letters representing atoms and bonds.*
FDA Label Image

Principal Display Panel (400 mg per 5 mL Bottle Label)

Principal Display Panel (400 mg per 5 mL Bottle Label)
Label for Erythromycin Ethylsuccinate oral suspension, USP, showing 200 mg per 5 mL strength when reconstituted. The label indicates a 100 mL suspension volume after mixing, with directions for mixing, storage instructions, dosage information, and manufacturer Wilshire Pharmaceuticals Inc. The label includes a barcode and the NDC 52536-132-13.*
FDA Label Image

Erythromycin 03

Erythromycin 03
Label for Erythromycin Ethylsuccinate oral suspension, USP with erythromycin activity 400 mg per 5 mL when reconstituted. The 100 mL bottle is for oral suspension use and is labeled by Wilshire Pharmaceuticals Inc. Directions for mixing and storage instructions are provided along with dosage information for children.*

* 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.