Carboprost Tromethamine Injection, Solution
Product Images NDC 71839-137

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 71839-137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Be Pharmaceuticals 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

Carton (Carbocartoncaplin)

Carton (Carbocartoncaplin)
Carton label for Carboprost Tromethamine Injection, USP 250 mcg/mL, an intramuscular injection. The label indicates a package size of 10 single-dose 1 mL vials. It includes storage instructions to refrigerate between 2° to 8°C and manufacturer information showing Caplin Steriles Limited in India with distribution by BE Pharmaceuticals Inc. in Cary, NC. The product is marked Rx Only and instructs to discard unused portions.*
FDA Label Image

Structure (Carbostrucaplin)

Structure (Carbostrucaplin)
Chemical structure of carboprost tromethamine, as indicated by the presence of relevant molecular groups and ions. The diagram displays the molecular framework including hydroxyl groups, methyl group, carboxylate ion, and tromethamine ion.*
FDA Label Image

Vial (Carbovialcaplin)

Vial (Carbovialcaplin)
Label for CARBOPROST TROMETHAMINE Injection, USP 250 mcg/mL in a 1 mL single-dose vial for intramuscular use. The label includes storage instructions, manufacturer and distributor details (BE Pharmaceuticals Inc.), and notes to discard unused portions. The NDC 71839-137 is visible along with batch and expiration sections.*

* 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.