Baclofen Tablet
Product Images NDC 70518-3115

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 Baclofen (NDC 70518-3115). 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

Baclofen 20mg 70518 3115 01

Baclofen 20mg 70518 3115 01
Baclofen is a prescription-only medication manufactured by Camber Pharma Inc. The medication requires proper storage within a moderate temperature range to ensure effectiveness. It has an NDC number of 70518-3115-01 and can be repackaged by RemedyRepack Inc. Detailed usage instructions are available in the package insert. It is important to keep Baclofen and all medications out of the reach of children. The expiration date and lot number are not available from the given text.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Baclofen is a prescription medication available only through a doctor’s prescription. It is manufactured by Camber Pharma and is kept by RemedyRepack Inc. The National Drug Code (NDC) # is 70518-3115-00 and the original NDC source is 31722-0999-10. The medication should be kept out of reach of children and stored at a temperature of 20-26°C (63-77°F), with temporary excursions allowed to 15-30°C (59-86°F). The package insert should be referred to for directions on usage. Lot number and expiration date are not provided.*
FDA Label Image

Struct (Struct)

* 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.