Terbinafine Tablet
Product Images NDC 70518-4421

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Terbinafine (NDC 70518-4421). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Terbinafine 250 mg oral tablets, repackaged by RemedyRepack Inc. The label shows a quantity of 90 tablets, round white tablets, and includes storage instructions and manufacturer information from Cipla Ltd, India. The label displays the NDC number 70518-4421 and dosage directions referring to an insert.*

FDA Label Image

Mm2 (Terbinafine 250mg 70518 4421 01)

Terbinafine Tablet 250 mg in a bottle label showing quantity of 45 tablets. Labeled as repackaged by RemedyRepack Inc., Indiana, PA. Instructions include storage temperature and child safety warnings. Manufactured by Cipla Ltd., Kurkumbh, India.*

FDA Label Image

Image 2 (Terbinafine Str)

Chemical structure of the active ingredient Terbinafine hydrochloride, showing its molecular framework with aromatic rings and side chains.*

FDA Label Image

Image 1 (Terbinafine Table)

A table comparing adverse events and discontinuation rates between Terbinafine tablets and placebo. It lists headache, gastrointestinal symptoms (diarrhea, dyspepsia, abdominal pain, nausea, flatulence), dermatological symptoms (rash, pruritus, urticaria), liver enzyme abnormalities, taste disturbance, and visual disturbance with corresponding percentages for each group.*

* 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.