Aminocaproic Acid Injection, Solution
Product Images NDC 0517-9120

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 Aminocaproic Acid (NDC 0517-9120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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.

Product Images & Figures Index

FDA Label Image

Container Label (Aminocaproic Acid Injection Usp 1)

Container Label (Aminocaproic Acid Injection Usp 1)
Aminocaproic Acid injection label, USP 250 mg/mL (5 g/20 mL) in a 20 mL multiple dose vial for intravenous infusion after dilution. The label includes dosing instructions, storage conditions, and manufacturer information for American Regent, Inc. Located in Shirley, NY. The label also shows barcode and lot/expiration placeholders.*
FDA Label Image

20 mL Cartong (Aminocaproic Acid Injection Usp 2)

20 mL Cartong (Aminocaproic Acid Injection Usp 2)
Aminocaproic Acid Injection USP 250 mg/mL (5 g/20 mL) label for intravenous infusion after dilution. The label notes multiple dose vials, each containing 20 mL, from American Regent, Inc. Dosage instructions, ingredients, storage conditions, and NDC 0517-9120-25 are included.*
FDA Label Image

Serialization Label (Aminocaproic Acid Injection Usp 3)

Serialization Label (Aminocaproic Acid Injection Usp 3)
A black-and-white 2D barcode above printed text showing lot number 0000, expiration date 01/2099, GTIN 00305179120253, and serial number 0 on a label. The label is plain white with no other visible branding or product information.*

* 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.