Famciclovir Tablet, Film Coated
Product Images NDC 0093-8119

4 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Famciclovir (NDC 0093-8119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva 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

Famciclovir Tablet Film Coated A077487 1

Famciclovir Tablet Film Coated A077487 1
Chemical structure diagram of famciclovir, showing its molecular bonds and arrangement of atoms.*
FDA Label Image

Famciclovir Tablet Film Coated A077487 2

Famciclovir Tablet Film Coated A077487 2
Label for Famciclovir Tablets 125 mg film-coated tablets by Teva Pharmaceuticals USA, Inc. The label indicates the product contains 30 tablets and includes dispensing instructions and storage conditions. It features a barcode, lot and expiration date fields, and a prominently displayed NDC number 0093-8117-56.*
FDA Label Image

Famciclovir Tablet Film Coated A077487 3

Famciclovir Tablet Film Coated A077487 3
Famciclovir Tablets 250 mg film-coated tablets label by Teva Pharmaceuticals USA, Inc. The label includes NDC 0093-8118-56 and states the package contains 30 tablets. It provides pharmacist dispensing instructions and storage information. The label also includes barcode and manufacturing details.*
FDA Label Image

Famciclovir Tablet Film Coated A077487 4

Famciclovir Tablet Film Coated A077487 4
Label for Famciclovir Tablets 500 mg by Teva Pharmaceuticals USA, Inc. The film-coated tablet packaging contains 30 tablets. The label includes storage instructions, warnings to keep out of reach of children, and barcodes. The NDC is 0093-8119-56, and the label advises dispensing with an attached patient information leaflet.*

* 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.