Gabapentin Tablet
Product Images NDC 50228-523

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 50228-523). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen Pharmaceuticals, 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

Image (Gabapentin01)

Chemical structure diagram of gabapentin, showing its amino acid-based molecular framework with a cyclohexane ring, amino group, and carboxylic acid group.*

FDA Label Image

Image (Gabapentin02)

A line graph comparing the percent of patients improved with gabapentin tablets versus placebo. The x-axis shows percent improvement in pain from baseline, and the y-axis shows percent of patients improved. Two lines are plotted, one for gabapentin tablets and one for placebo, showing differences in patient improvement rates.*

FDA Label Image

300 mg (Gabapentin03)

Gabapentin 300 mg oral tablets label from ScieGen Pharmaceuticals, Inc. The label states each tablet contains 300 mg gabapentin and provides storage instructions, dosage administration notes, and a caution against interchanging with other gabapentin products. The package contains 90 tablets and is for prescription use only. The label includes the NDC 50228-523-90 and a barcode.*

FDA Label Image

600 mg (Gabapentin04)

Gabapentin 600 mg oral tablets label from ScieGen Pharmaceuticals, Inc. The label indicates the dosage strength as 600 mg and contains 90 tablets per bottle. It includes storage instructions, usage cautions, and a barcode. The label states the product is Rx only and notes it is once-daily dosing with no varnish.*

* 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.