Prochlorperazine Maleate Tablet, Film Coated
Product Images NDC 59651-774

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prochlorperazine Maleate (NDC 59651-774). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label.principal Display Panel- 5 mg (100 Tablets Bottle) (Prochlorperazine Fig1)

Label for Prochlorperazine Maleate Tablets USP 5 mg, film-coated oral tablets, packaged as 100 tablets. The label indicates prescription use only and includes storage instructions, dosage information, and distributor details for Aurobindo Pharma USA, Inc. The tablet imprint is a single-digit '5'. The product is made in India by Aurobindo Pharma Limited.*

FDA Label Image

Package Label.principal Display Panel- 10 mg (100 Tablets Bottle) (Prochlorperazine Fig2)

Label for prochlorperazine maleate tablets, USP 10 mg oral film-coated tablets. The label shows a container with 100 tablets, produced by Aurobindo Pharma Limited. It includes dosage information, storage instructions, distributor details, and a barcode. The label highlights the 10 mg strength and features a yellow tablet imprint with 'PZ' and '10'.*

FDA Label Image

Chemical Structure (Prochlorperazine Str)

Chemical structure of prochlorperazine maleate, showing the molecular arrangement of its components including a phenothiazine core with a chlorine substituent and the maleate part as a dicarboxylic acid moiety.*

* 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.