Flecainide Acetate Tablet
Product Images NDC 76385-145

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Flecainide Acetate (NDC 76385-145). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unichem Pharmaceuticals (usa), 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

Fpl-bl-100mg-60tabs-06.jpg (100mg Label)

Flecainide Acetate Tablets, USP 100 mg oral tablet label. The label indicates 60 tablets per container, distributed by Bayshore Pharmaceuticals LLC and manufactured by Beximco Pharmaceuticals Ltd. Storage instructions specify maintaining 20°C to 25°C (68°F to 77°F). The label includes an NDC of 76385-146-60.*

FDA Label Image

Fpl-bl-150mg-60tabs-06.jpg (150mg Label)

Label for Flecainide Acetate Tablets USP, 150 mg oral tablets. The label indicates a 60 tablet count and features branding for Bayshore Pharmaceuticals as the distributor and Beximco Pharmaceuticals Ltd. as the manufacturer. Storage instructions and dosage referencing are also present.*

FDA Label Image

Fpl-bl-50mg-60tabs-06.jpg (50mg Label)

Flecainide Acetate Tablets, USP, 50 mg oral tablets. The label shows the product name and strength prominently, distributed by Bayshore Pharmaceuticals LLC and manufactured by Beximco Pharmaceuticals Ltd. The package contains 60 tablets and includes storage instructions and NDC 76385-145-60.*

FDA Label Image

Flecainide Structural Formula (Structure)

Chemical structure of flecainide acetate showing its molecular framework, including a piperidine ring, amide linkage, and trifluoromethoxy substituents on a benzene ring.*

* 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.