Tranexamic Acid Tablet
Product Images NDC 72578-220

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tranexamic Acid (NDC 72578-220). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona 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

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Tranexamic Acid 650 mg oral tablets packaged in a white and blue blister card. The blister card has four tablets arranged in two rows, with dosing information and manufacturer Viona Pharmaceuticals Inc indicated on the card.*

FDA Label Image

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Chemical structure diagram of the active ingredient Tranexamic Acid showing its molecular configuration with amino, carboxyl, and cyclohexane components.*

FDA Label Image

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A line graph depicting mean menstrual blood loss (mL) over a treatment period spanning six cycles, comparing Tranexamic Acid 3900 mg/day versus placebo. Data are shown separately for 3-cycle and 6-cycle studies, with mean blood loss values plotted for baseline and each cycle.*

FDA Label Image

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Tranexamic Acid 650 mg oral tablets in a silver blister pack containing 10 tablets arranged in two rows of five. The pack is marked with the proprietary name, strength, and the labeler Viona Pharmaceuticals Inc in black text on the silver foil background.*

FDA Label Image

650 mg (B8613d4e 453f 4f45 82c8 50803881383b 03)

Tranexamic Acid Tablets USP 650 mg oral tablets, packaged in a container of 30 tablets. The label shows the proprietary name Tranexamic Acid, strength 650 mg, and specifies Rx only. It also includes manufacturer and distributor information: manufactured by Zydus Pharmaceuticals Ltd, India, and distributed by Viona Pharmaceuticals Inc, Cranford, NJ.*

* 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.