Terbinafine Tablet
Product Images NDC 60687-909

View Photos of 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 Terbinafine (NDC 60687-909). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

250 mg Terbinafine Tablet Blister.jpg (250 mg Terbinafine Tablet Blister)

250 mg Terbinafine Tablet Blister.jpg (250 mg Terbinafine Tablet Blister)
Sheet of multiple Terbinafine Tablet, USP 250 mg labels from American Health Packaging. Each label shows the product name, strength, dosage form, a barcode, and space for lot number and expiration date. Labeler information and NDC 60687-909 are also visible.*
FDA Label Image

250 mg Terbinafine Tablets Carton.jpg (250 mg Terbinafine Tablets Carton)

250 mg Terbinafine Tablets Carton.jpg (250 mg Terbinafine Tablets Carton)
Terbinafine Tablets USP 250 mg oral tablets in a package containing 30 tablets (3 blister packs of 10). Label shows the NDC 60687-909-21 by American Health Packaging. The label includes directions for pharmacists to dispense with a medication guide and storage instructions.*
FDA Label Image

Ahp90921

Ahp90921
Terbinafine 250 mg oral tablet, round and white, imprinted with 'D' on one side and '74' on the other. This prescription drug is labeled by American Health Packaging.*
FDA Label Image

Chemical Structure (Terbinafine Str)

Chemical Structure (Terbinafine Str)
Chemical structure of Terbinafine Hydrochloride depicting its molecular arrangement, including aromatic rings and aliphatic chains with hydrochloride indicated.*

* 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.