Gabapentin Tablet
Product Images NDC 63629-8491

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 63629-8491). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Figure 1 (Image 01)

Figure 1 (Image 01)
This appears to be a table showing the mean pain score for different treatments over a period of weeks. The treatments mentioned are Parkod with either a titration or fixed dose, placebo, and Gabapentin at a dosage of 3600 mg/day. Both baseline and weeks are mentioned, indicating that the pain scores were tracked over a period of time.*
FDA Label Image

Figure 2 (Image 02)

Figure 2 (Image 02)
This is a chart showing the results of a 4-week fixed dose period study on the effectiveness of Gabapentin in reducing pain. The x-axis represents the weeks of the study, while the y-axis represents the mean pain score reported by participants. The study included a placebo group as well as groups taking 1800 mg/day and 2400 mg/day of Gabapentin. The chart shows a decrease in pain score over time in both Gabapentin groups compared to the placebo group.*
FDA Label Image

Figure 3 (Image 03)

FDA Label Image

Image-04 (Image 04)

FDA Label Image

Gabapentin Structural Formula (Image 05)

FDA Label Image

Image-09 (Image 09)

FDA Label Image

Label (Lbl636298491)

Label (Lbl636298491)
Gabapentin Tablets, USP 600 mg used in treating seizures and nerve pains. Each film-coated tablet contains 600 mg of gabapentin, USP. The tablets must be kept away from the reach of children and stored at 20°C to 25°C. The tablets should be dispensed in a tight container with a child-resistant closure. The National Drug Code for this medication is 63629-8491-1, and it is available in the market in the packet of 500 Tablets with the prescription of a doctor.*

* 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.