Terbinafine Hydrochloride Tablet
Product Images NDC 70518-3907

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Terbinafine Hydrochloride (NDC 70518-3907). 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.

Product Images & Figures Index

FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Terbinafine is available in the form of 250 mg tablets. The prescription medication is intended for oral use and comes in a quantity of 90 tablets. The packaging advises protecting it from light. The medication should be stored at a temperature between 20-25°C (58-77°F), with excursions permitted to 15-30°C (59-86°F). The prescription is only available with a doctor's prescription. The National Drug Code (NDC) for this product is 70518-3807-00, and the source NDC is 69452-0351-20. The manufacturer, Bienpharma Inc, is located in Princeton, NJ 08540. The Medication should be kept out of the reach of children. The medication was repackaged by RemedyRepack inc., located in Indiana, PA 15701. Further direction for use can be found in the package insert. The expiration date and lot number are not provided in the given text.*
FDA Label Image

Mm2 (Terbinafine 250mg 70518 3907 01)

Mm2 (Terbinafine 250mg 70518 3907 01)
Terbinafine 250 mg Tablet is available in a quantity of 30 tablets. It is a prescription medication that is used for certain fungal infections. It should be stored away from light and at a temperature of 20-25°C (58-77°F), with excursions permitted to 15.30°C (59-86°F). The medication is manufactured by Bienpharma Inc, located in Princeton, NJ 08540. It is important to keep this medication out of the reach of children. The Rx only label indicates that it requires a prescription. The National Drug Code (NDC) for this product is 70518-3007-01, and the Lot number and expiration date are not available from the provided text. Additionally, it appears that the medication has been repackaged by RemedyRepack Inc, located in Indiana, PA 15701. For proper usage instructions, please refer to the package insert.*
FDA Label Image

Structure (Terbinafine Tablets Figure 1)

Structure (Terbinafine Tablets Figure 1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.