Dihydroergotamine Mesylate Injection, Solution
Product Images NDC 36000-300

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dihydroergotamine Mesylate (NDC 36000-300). 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

1mg-1ml-carton (1mg 1ml Carton)

Packaging label for Dihydroergotamine Mesylate Injection, USP 1 mg/mL by Baxter Healthcare Corporation. The label specifies it is for intravenous, intramuscular, and subcutaneous use, containing 10 single-dose 1 mL ampules. Instructions for use illustrating ampule opening are included. Storage and manufacturing information are provided, as well as dosage and ingredient details.*

FDA Label Image

1mg-1ml-label (1mg 1ml Label)

Label for dihydroergotamine mesylate injection, USP 1 mg/mL in a 1 mL single-dose ampule. The solution is for intravenous, intramuscular, and subcutaneous use. Manufactured for Baxter Healthcare Corporation, Deerfield, IL, made in Germany. Includes NDC 36000-300-01 barcode, lot, and expiration placeholders.*

FDA Label Image

Instructions-for-use (Instructions For Use)

Illustration showing how to open a one-point-cut ampule. The left image highlights the ampule's neck with the cut below it. The right image demonstrates placing the thumb on the neck and snapping the top back to break the ampule open.*

FDA Label Image

Structural-formula-dihydroergotamine-mesylate (Structural Formula Dihydroergotamine Mesylate)

Chemical structure of dihydroergotamine mesylate, depicting its molecular arrangement including the ergot alkaloid core and the mesylate group.*

* 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.