Gabapentin Tablet
Product Images NDC 68382-355

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 68382-355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals 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

Image (78022efd 887c 48c9 Af64 A6b5426a9fbf 01)

Chemical structure diagram of gabapentin showing a cyclohexane ring attached to an amino group and a carboxylic acid functional group.*

FDA Label Image

Image (78022efd 887c 48c9 Af64 A6b5426a9fbf 02)

A line graph comparing percent improvement in pain from baseline (x-axis) against percent of patients improved (y-axis) for gabapentin versus placebo. Two lines are shown, with gabapentin consistently showing a higher percentage of patients improved across varying levels of pain improvement.*

FDA Label Image

300 mg (78022efd 887c 48c9 Af64 A6b5426a9fbf 03)

Label for Gabapentin Tablets 300 mg, oral dosage form, manufactured by Zydus Pharmaceuticals USA Inc. The package contains 90 film-coated tablets with once-daily dosing. The label includes directions, storage conditions, pharmacist instructions, and regulatory information including the NDC code 68382-608-16.*

FDA Label Image

600 mg (78022efd 887c 48c9 Af64 A6b5426a9fbf 04)

Gabapentin Tablets 600 mg oral dosage form shown in a product label by Zydus Pharmaceuticals USA Inc. The label indicates a once-daily administration with 90 tablets per container. It includes usage instructions, storage conditions, and cautionary statements, emphasizing not to interchange with other gabapentin products. This is a prescription-only medication.*

* 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.