Prochlorperazine Edisylate Injection
Product Images NDC 43066-090

3 FDA label images from Baxter Healthcare Corporation · 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 Edisylate (NDC 43066-090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Structural Formula (Image 01)

Structural Formula (Image 01)
Chemical structure diagram of prochlorperazine edisylate showing molecular components and arrangement, including aromatic rings, chlorine atom, and sulfonate groups.*
FDA Label Image

2ml-vial-label (2ml Vial Label)

2ml-vial-label (2ml Vial Label)
Label for PROCHLORPERAZINE EDISYLATE Injection, USP, 5 mg/mL strength, in a 2 mL multiple-dose vial. The label indicates the product is for deep intramuscular or intravenous use only, not for subcutaneous use. Manufactured by Caplin Steriles Limited in India and distributed by Baxter Healthcare Corporation, Deerfield, IL.*
FDA Label Image

2ml-carton-label (2ml Carton Label)

2ml-carton-label (2ml Carton Label)
Prochlorperazine Edisylate Injection, USP 10 mg/2 mL (5 mg/mL) multi-dose vials packaging label by Baxter Healthcare Corporation. The label states administration routes as deep intramuscular or intravenous use only, not for subcutaneous use, and advises protection from light. The label includes NDC 43066-090-25 and lists manufacturing by Caplin Steriles Limited, India, with distribution by Baxter Healthcare Corporation, Deerfield, IL.*

* 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.