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.

Product Images & Figures Index

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

Representative Vial Label (Image 02)

Representative Vial Label (Image 02)
Label for Prochlorperazine Edisylate Injection, USP, 10 mg/2 mL (5 mg/mL) in a 2 mL multiple-dose vial. The injection is for deep intramuscular or intravenous use only, not for subcutaneous use. The label shows the NDC 43066-090-01, and the product is distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, with lot and expiration information fields visible.*
FDA Label Image

Representative Carton Label (Image 03)

Representative Carton Label (Image 03)
Packaging label for PROCHLORPERAZINE EDISYLATE Injection, USP 10 mg/2 mL (5 mg/mL) by Baxter Healthcare Corporation. The label states the drug is for deep intramuscular or intravenous use only, not for subcutaneous use, and includes storage and usage warnings. The package contains 25 multi-dose 2 mL vials. Baxter is identified as the labeler.*

* 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.