Hemabate Injection, Solution
Product Images NDC 0009-0856

4 FDA label images from Pharmacia & Upjohn Company Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hemabate (NDC 0009-0856). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharmacia & Upjohn Company 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

Chemical Structure (Hemabate 01)

Chemical Structure (Hemabate 01)
Chemical structure of carboprost tromethamine, the active ingredient in Hemabate injection, solution 250 ug/mL by Pharmacia & Upjohn Company LLC. The structure shows the molecular arrangement with functional groups and the tromethamine counterion.*
FDA Label Image

Logo (Hemabate 02)

FDA Label Image

Principal Display Panel (1 mL Ampule Label)

Principal Display Panel (1 mL Ampule Label)
Hemabate 250 mcg intramuscular injection label shows the proprietary name with generic name carboprost tromethamine. The label specifies 1 mL ampule, instructs refrigeration at 2° to 8°C, and highlights it is for intramuscular use only. Distributed by Pharmacia & Upjohn Company LLC, a Pfizer division, with lot and expiration placeholders.*
FDA Label Image

Principal Display Panel (10 Single-Dose Ampoule Carton)

Principal Display Panel (10 Single-Dose Ampoule Carton)
The packaging label for Hemabate carboprost tromethamine injection, USP, 250 mcg per 1 mL single-dose ampules. The label indicates intramuscular use only and displays the Pfizer Injectables logo. It includes storage instructions to refrigerate between 2° to 8°C, a barcode, and details about the contents and preservatives.*

* 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.