Flecainide Acetate Tablet
Product Images NDC 65162-643

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Flecainide Acetate (NDC 65162-643). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

D980fd55-figure-01 (Flecainide Acetate Tablets 1)

Chemical structure diagram of flecainide acetate, showing its molecular configuration with annotated atoms and bonds typical for this active pharmaceutical ingredient.*

FDA Label Image

50 mg Label (Flecainide Acetate Tablets 2)

Label for Flecainide Acetate Tablets USP, 50 mg, oral tablets from Amneal Pharmaceuticals LLC. The label indicates the product is available by prescription only, contains 100 tablets, and instructs to store at 20 to 25°C (68 to 77°F). It features dosage strength and manufacturer information along with handling and storage instructions.*

FDA Label Image

100 mg Label (Flecainide Acetate Tablets 3)

Flecainide Acetate Tablets, USP 100 mg oral tablets in a bulk package of 100 tablets from Amneal Pharmaceuticals LLC. The label includes dosage strength, NDC 65162-642-10, storage instructions at 20° to 25°C, and a barcode.*

FDA Label Image

150 mg Label (Flecainide Acetate Tablets 4)

Flecainide Acetate Tablets, USP 150 mg oral tablet label. The label shows 100 tablets in the package, labeled for prescription use only from Amneal Pharmaceuticals LLC. It includes dosage strength, storage conditions (20° to 25°C), and a barcode. The label states it is a bulk package with warnings to keep out of reach of children.*

* 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.