Prochlorperazine Maleate Tablet, Film Coated
Product Images NDC 62135-674

View Photos of 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 Prochlorperazine Maleate (NDC 62135-674). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

Image Description (Prochlorperazine Maleate 10mg Bottle Label)

Image Description (Prochlorperazine Maleate 10mg Bottle Label)
Packaging label for Prochlorperazine Maleate tablets USP, 10 mg strength, film-coated tablets. The label indicates Rx only with a quantity of 90 tablets. The labeler is Chartwell RX, LLC. Features include dosage information, safety warnings, storage instructions, and a barcode with NDC 62135-674-90.*
FDA Label Image

Image Description (Prochlorperazine Maleate 5mg Bottle Label)

Image Description (Prochlorperazine Maleate 5mg Bottle Label)
Prochlorperazine Maleate 5 mg film-coated tablets packaging label. The label shows the product name, strength of 5 mg, dosage form as tablets USP, and that the package contains 90 tablets. It is labeled Rx Only and manufactured by Chartwell RX, LLC. The label includes usage and storage instructions along with a barcode and NDC 62135-673-90.*
FDA Label Image

Image Description (Prochlorperazine Maleate Structure)

Image Description (Prochlorperazine Maleate Structure)
Chemical structure diagram of prochlorperazine maleate showing the molecular arrangement including a piperazine ring, chlorinated phenothiazine core, and maleate counter ion.*

* 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.