Gabapentin
Product Images NDC 61919-350

3 FDA label images from Direct_rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 61919-350). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

417 60

417 60
Packaging label for GABAPENTIN 300 mg capsules, containing 60 capsules. The label identifies it as a generic for Neurontin and notes each capsule contains 300 mg of gabapentin. The label includes lot number, expiration date of 04/19, barcode, and manufacturer/distributor Direct_Rx in Alpharetta, GA. NDC code 61919-417-60 is displayed.*
FDA Label Image

661 90

661 90
Label for Gabapentin 100 mg capsules, package of 90 capsules, labeled as generic for Neurontin. The label indicates each capsule contains 100 mg of gabapentin and is packaged and distributed by Direct Rx. The label also includes lot and expiration details, barcode, and usage warnings.*
FDA Label Image

Gabapentin 800mg (Gabapentin 800mg)

Gabapentin 800mg (Gabapentin 800mg)
GABAPENTIN 800 mg, 90 tablet bottle label. The label states it is generic for Neurontin and each tablet contains 800 mg of gabapentin USP. The product is packed and distributed by Direct Rx in Alpharetta, GA. The label includes lot number, discard after date, dosage instructions with warnings to keep out of reach of children, and an NDC barcode with number 61919-350-90.*

* 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.