Prochlorperazine Edisylate Injection
Product Images NDC 65145-119

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Prochlorperazine Edisylate (NDC 65145-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caplin Steriles 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

Image1 (Prochlorperazine 1)

Chemical structure of Prochlorperazine Edisylate, showing its molecular formula C20H24ClN3S with additional sulfonic acid components, and a molecular weight of 564.14.*

FDA Label Image

Image-2 (Prochlorperazine 2)

Label for Prochlorperazine Edisylate Injection, USP, 10 mg/2 mL (5 mg/mL) in a 2 mL multiple-dose vial. The label indicates use for deep intramuscular or intravenous injection only and not for subcutaneous use. Manufactured by Caplin Steriles Limited. Contains NDC 65145-119-01.*

FDA Label Image

Image-3-2 (Prochlorperazine 3 1)

Label for Prochlorperazine Edisylate Injection, USP, 10 mg/2 mL (5 mg/mL) by Caplin Steriles Limited. The label indicates the drug is for deep intramuscular or intravenous use only, not for subcutaneous use, and should be protected from light. The package contains 25 multiple-dose vials of 2 mL each.*

FDA Label Image

Image-3-1 (Prochlorperazine 3 2)

Packaging label for Prochlorperazine Edisylate Injection, USP 10 mg/2 mL (5 mg/mL) by Caplin Steriles Limited, NDC 65145-119-25. The label indicates use for deep intramuscular or intravenous injection only, not for subcutaneous use, and states to protect from light. The packaging includes a 25 x 2 mL multiple-dose vial configuration. Storage instructions and dosage information references are partially visible.*

* 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.