Fanatrex
Product Images NDC 43093-105

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fanatrex (NDC 43093-105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by California Pharmaceuticals Llc, 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

Fanatrex Box (1 Fanatrex Carton)

Fanatrex gabapentin 25 mg/mL oral suspension kit packaging label by California Pharmaceuticals LLC, NDC 43093-105. The label indicates this is a FusePaq™ kit for oral suspension containing gabapentin. Storage instructions note room temperature (15-30°C). The kit includes active and inactive bulk materials to prepare 420 mL of suspension, with listed inactive ingredients and components like a disposable funnel and oral dispenser. The label also advises the product is Rx only and includes a barcode.*

FDA Label Image

Gabapentin Label (2 Gabapentin Label)

Partial label of Fanatrex showing the active ingredient Gabapentin with its chemical name and CAS number. The label includes a caution for manufacturing, processing, repacking, or prescription compounding. Net contents are 10.5 g. The product is repackaged by Fusion Pharmaceuticals, LLC in Camarillo, CA.*

FDA Label Image

Suspension Label (3 Suspension Label)

Text panel for Fanatrex Oral Suspension Vehicle from California Pharmaceuticals LLC, labeled for prescription compounding only. It lists the product as dye and paraben free, includes ingredients such as water, banana and strawberry flavors, and other excipients, and states a net content of 420 mL (14.2 fl oz). Manufactured for Fusion Pharmaceuticals, LLC, Camarillo, CA.*

* 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.