Flecainide Acetate Tablet
Product Images NDC 51407-019

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Flecainide Acetate (NDC 51407-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

Flecainide (Flecainide)

Chemical structure of Flecainide Acetate, showing its molecular formula details including trifluoromethoxy and methyl groups, a piperidine ring, and amide linkage.*

FDA Label Image

Ani (Ani)

FDA Label Image

51407-018-01ol (Flecainide Acetate)

Label for Flecainide Acetate Tablets, USP 50 mg oral tablets. The label shows the product name, strength, and package size of 100 tablets. It includes the NDC 51407-018-01 and is marketed by GSMS, Incorporated in Camarillo, CA. Additional details mention dosage instructions and storage conditions.*

FDA Label Image

51407-019-01ol (Flecainide Acetate)

The label for Flecainide Acetate Tablets USP displays the 100 mg strength in a blue box. The package contains 100 tablets and is marked Rx Only. The label includes the NDC number 51407-019-01 and states the product is marketed by GSMS, Incorporated, Camarillo, CA. Storage and dispensing instructions are also provided.*

FDA Label Image

51407-020-01ol (Flecainide Acetate)

Flecainide Acetate Tablets USP 150 mg label showing the NDC number 51407-020-01. The label includes a barcode, product name, strength, and count of 100 tablets. It notes keep out of reach of children and storage between 20°-25°C. Marketed by GSMS, Incorporated, Camarillo, CA. Rx only.*

* 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.