Erythromycin Tablet, Delayed Release
Product Images NDC 52536-180

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Erythromycin (NDC 52536-180). 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.

FDA Label Image

Chemical Structure (Erythromycin 01)

Chemical structure diagram of erythromycin, showing its molecular framework with multiple rings, including lactone rings, sugar moieties, and functional groups such as hydroxyl and methyl groups.*

FDA Label Image

Principal Display Panel (250 mg Tablet Bottle Label)

Label for Erythromycin delayed-release tablets, USP, 250 mg strength, oral dosage form. The label shows a carton or bottle label with the NDC 52536-180-03, containing 30 tablets. The product is enteric-coated and labeled as prescription only from Wilshire Pharmaceuticals.*

FDA Label Image

Principal Display Panel (333 mg Tablet Bottle Label)

Label for Erythromycin delayed-release tablets, USP, 333 mg strength. The label indicates 30 tablets per container, enteric-coated, and includes the NDC 52536-183-03. It is manufactured by Wilshire Pharmaceuticals, Inc., Atlanta, GA. Storage and handling instructions are also provided.*

FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Label for Erythromycin delayed-release tablets, 500 mg strength, by Wilshire Pharmaceuticals. The label indicates the product is a USP enteric-coated tablet available in a 30-tablet container. Storage instructions and dispensing warnings are included, along with the NDC 52536-186-03.*

* 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.