Gabapentin
Product Images NDC 67296-1745

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 67296-1745). 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.

FDA Label Image

Label (67296 1745)

Label for Gabapentin 800 mg tablets, 60 count, NDC 67296-1745-6. The label includes the Rx Only designation, lot number 178112X1, and expiration date 07/21. Manufacturer is Sciegen Pharmaceuticals Inc, Hauppauge, NY, and the distributor is RedPharm Drug, Eden Prairie, MN. Storage instructions advise controlled room temperature (20-25°C).*

FDA Label Image

Clcr Calculation (Spl Image1 Clcr Calc)

An illustration showing the formula for calculating creatinine clearance (CLCr) involving age, weight, serum creatinine, and an adjustment factor for female patients.*

FDA Label Image

Structure (Spl Image2 Structure)

Chemical structure of gabapentin, illustrating its molecular arrangement with a cyclohexane ring connected to an amino group (CH2NH2) and a carboxyl group (CH2CO2H).*

FDA Label Image

Figure (Spl Image3 Figure)

A scatter plot illustrating the percentage difference in outcomes across three studies (a, b, and c) plotted against various daily doses of gabapentin in milligrams (600, 900, 1200, 1800 mg). The difference percentage is shown on the vertical axis, while the daily dose (mg) is on the horizontal axis, with distinct markers for each study.*

FDA Label Image

Label 600 mg (Spl Image4 Label 600mg)

Label of Gabapentin Tablets, USP 600 mg by RedPharm Drug, Inc. The label shows 500 tablets per container. Storage instructions advise keeping at 20° to 25°C with allowed excursions. The label includes usual dosage directions to read prescribing information, warnings to keep out of reach of children, and instructions to dispense in a child-resistant closure. Manufacturer info lists ScieGen Pharmaceuticals, Inc., Hauppauge, NY and distributor Solco Healthcare, LLC, Cranbury, NJ. NDC 43547-389-50 is printed.*

FDA Label Image

Label 800 mg (Spl Image5 Label 800mg)

GABAPENTIN 800 mg film-coated tablets packaging label. The product contains 500 tablets, labeled as Tablets, USP. The label includes storage instructions, manufacturer (ScieGen Pharmaceuticals, Inc.), and distributor (Solco Healthcare, LLC). The label also displays NDC 43547-390-50 and notes the product is Rx only. The labeler is RedPharm Drug, Inc.*

FDA Label Image

Label 100mg (Spl Label 100mg)

Label for Gabapentin Capsules, USP 100 mg, in a bottle of 100 capsules. The label includes storage instructions, dosage guidance to read prescribing information, bar code, and manufacturer details: ScieGen Pharmaceuticals, Inc., manufactured for Solco Healthcare U.S., LLC. The design features a blue and red color scheme with the NDC 43547-383-10.*

FDA Label Image

Label 300mg (Spl Label 300mg.jpg.jpg)

Label for Gabapentin Capsules USP 300 mg, showing product name, dosage strength, and form. The label states a count of 100 capsules and includes storage instructions, a barcode, and manufacturer information (ScieGen Pharmaceuticals, Inc.) with the labeler listed as Solco Healthcare U.S., LLC. It features a blue color scheme with white and light blue text.*

FDA Label Image

Label 400mg (Spl Label 400mg.jpg.jpg)

Label for Gabapentin Capsules, USP 400 mg, showing a package of 100 capsules. The label includes the NDC number 43547-385-10 and instructions for storage and dispensing. It lists ScieGen Pharmaceuticals, Inc. as the manufacturer and Solco Healthcare U.S., LLC as the manufacturer for. The label also contains cautionary notes on storage temperature and keeping medication out of children’s reach.*

* 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.