Gabapentin Tablet
Product Images NDC 76420-235

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 76420-235). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

Gabapentin-600mg (Gabapentin 600mg)

Gabapentin Tablets are included in this text, with different NDCs and quantities ranging from 30 to 240 in a single package. The text also includes the description, drug status, lot, batch number, and caution for each package. The drug is only dispensed with a prescription, and the package should be kept away from children and stored at controlled room temperature.*

FDA Label Image

Figure 1 (Image 01)

This text appears to be a table or chart, showing mean pain score at baseline and during weeks of a study involving two different dosing regimens for a medication called "Parkod" and a placebo or gabapentin. The format of the table is not clear without additional context, but it seems to be comparing the effects of the different doses on pain.*

FDA Label Image

Figure 2 (Image 02)

This appears to be a chart or graph showing the results of a study on the effects of different doses of Gabapentin on pain scores over a 4-week period, including a placebo group. The x-axis represents the weeks of the study, and the y-axis represents the mean pain score. The study included a baseline measurement and two different doses of Gabapentin (1800mg/day and 2400mg/day).*

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-06 (Image 06)

* 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.