Carboprost Tromethamine Injection, Solution
Product Images NDC 65219-579

View Photos of 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 Carboprost Tromethamine (NDC 65219-579). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Carboprost-spl-structure (Car13 0000 01)

Carboprost-spl-structure (Car13 0000 01)
Chemical structure of carboprost tromethamine, showing its molecular arrangement including hydroxyl groups, double bonds, and the tromethamine counterion.*
FDA Label Image

Fresenius Kabi Logo (Car13 0000 02)

FDA Label Image

Package Label Principal Display Panel (Car13 0000 03)

Package Label Principal Display Panel (Car13 0000 03)
Label for CARBOPROST TROMETHAMINE Injection, USP 250 mcg/mL, an intramuscular injection solution in a 1 mL single-dose vial. The label indicates refrigeration at 2° to 8°C and instructs to discard unused portions. Manufactured by Fresenius Kabi USA, LLC, with origin in India. The label includes the product's NDC 65219-579-00.*
FDA Label Image

Package Label.principal Display Panel (Car13 0000 04)

Package Label.principal Display Panel (Car13 0000 04)
Packaging label for Carboprost Tromethamine Injection, USP 250 mcg/mL by Fresenius Kabi USA, LLC. The product is an intramuscular injection solution supplied in 10 single-dose 1 mL vials. The label includes dosage strength, usage instructions, storage conditions, batch overprinting area, manufacturer information, and 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.