Carboprost Tromethamine Injection, Solution
Product Images NDC 0409-0064

View Photos of 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 Carboprost Tromethamine (NDC 0409-0064). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, Inc., 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

Carboprost-spl-carton (Carboprost Spl Carton)

Carboprost-spl-carton (Carboprost Spl Carton)
Packaging label for Carboprost Tromethamine Injection, USP, 250 mcg/mL, for intramuscular use only. The carton contains 10 single-dose 1 mL vials. Distributed by Hospira, Inc., the label includes storage instructions at 2° to 8°C and notes that the product is made in India. The label features dosing information and warnings, with the NDC codes 0409-0064-10 and 0409-0064-01.*
FDA Label Image

Structure (Carboprost Spl Structure)

Structure (Carboprost Spl Structure)
Chemical structure of carboprost tromethamine, showing its molecular components and ionic form with tromethamine.*
FDA Label Image

Carboprost-spl-vial (Carboprost Spl Vial)

Carboprost-spl-vial (Carboprost Spl Vial)
Label for Carboprost Tromethamine Injection, USP 250 mcg/mL in a 1 mL single-dose vial. The label states for intramuscular use only, Rx only, and includes storage instructions to refrigerate at 2° to 8°C (36° to 46°F). Distributed by Hospira, Inc., Lake Forest, IL, USA, the label also shows the NDC 0409-0064-01 and features a barcode.*

* 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.