Fluvoxamine Maleate Tablet, Film Coated
Product Images NDC 69452-289

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluvoxamine Maleate (NDC 69452-289). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Principal Display Panel (25 mg)

Label for Fluvoxamine Maleate Tablets, USP 25 mg by Bionpharma Inc. The label indicates a package size of 100 tablets for oral use under prescription (Rx only). It includes storage instructions, a pharmacist dispensing note, and a barcode. The product is made in India and distributed by Bionpharma Inc., Princeton, NJ.*

FDA Label Image

Principal Display Panel (50 mg Tablet)

Fluvoxamine Maleate Tablets, USP 50 mg oral tablets in a bottle of 100 count. The label displays the active ingredient and strength prominently, along with the distributor as Bionpharma Inc. The label includes storage instructions and a barcode on the right side, with the product identified as prescription only.*

FDA Label Image

Principal Display Panel (100 mg Tablet)

Label for Fluvoxamine Maleate Tablets USP 100 mg oral tablets, packaged as 100 tablets per bottle. The label indicates it is a prescription drug distributed by Bionpharma Inc. The label includes dosage and storage instructions, child-resistant packaging information, and origin marked as Made in India.*

FDA Label Image

Chemical Structure (Structure001)

Chemical structure diagram showing the molecular arrangement of fluvoxamine maleate, the active ingredient in Fluvoxamine maleate tablets by Bionpharma Inc.*

* 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.