Gabapentin
Product Images NDC 67296-1638

3 FDA label images from Redpharm Drug, Inc. · 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 67296-1638). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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.

Product Images & Figures Index

FDA Label Image

Gabapentin 1638 6

Gabapentin 1638 6
Label for Gabapentin 300 mg capsules, bottle containing 60 capsules. The label shows the NDC 67296-1638-6 and states "Rx Only." Manufacturer is Marksans Pharma Ltd, located in Verna Goa, India. Distributed by RedPharm Drug, Eden Prairie, MN. Includes lot number G006FX1 and expiration date 12/20.*
FDA Label Image

Label (Sdistributi19051413090 0001)

Label (Sdistributi19051413090 0001)
Label for GABAPENTIN 300MG capsules, containing 20 capsules. The label includes the NDC number 67296-1638-2, the note Rx Only, and storage instructions at controlled room temperature (20-25°C). The product is manufactured by Marksans Pharma Limited in India and distributed by RedPharm Drug, Inc. in Eden Prairie, MN.*
FDA Label Image

Gab Medguide (Gab Medguide)

Gab Medguide (Gab Medguide)
Medication guide text for Gabapentin capsules by RedPharm Drug, Inc. The guide includes warnings about serious side effects such as suicidal thoughts, allergic reactions, and behavioral changes. It lists important safety information, instructions for use, possible side effects, storage recommendations, and information on the prescription status. Additional details include advice on pregnancy, breastfeeding, and interactions with other medicines.*

* 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.