Gabapentin Tablet
Product Images NDC 72189-178

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 72189-178). 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.

FDA Label Image

72189-158-30 (72189 158 30)

Gabapentin 800 mg oral capsules, 30 count bottle label by Direct Rx. The label indicates the capsules are generic for Neurontin and are film-coated tablets containing 800 mg of gabapentin. It includes NDC numbers, lot number, manufacturing and expiration dates, and packaging details.*

FDA Label Image

Hi (72189 178 72)

GABAPENTIN 800 mg oral capsules, 120 count, packaged and distributed by DIRECT RX. Label indicates it is generic for Neurontin, with each film-coated tablet containing 800 mg of gabapentin, USP. Information includes lot number, expiration date 7/31/23, and manufacturing details by SciGen Pharmaceuticals, Inc.*

FDA Label Image

Hi (72189 109 72)

GABAPENTIN 100 mg capsule label for 120 capsules, generic for Neurontin, distributed by Direct Rx. The label includes the NDC number 72189-109-72, lot number SAMPLE, expiration date 11/30/21, and manufacturing information. It also features cautionary text on storage and prescription transfer restrictions.*

FDA Label Image

Hi (72189 109 90)

Gabapentin 100 mg oral capsules, 90 count, packaged and distributed by Direct Rx. The label states it is a generic for Neurontin and includes lot number 08JN2004 with an expiration date of 3/31/22. The label also includes manufacturer and NDC information, along with warnings and storage instructions.*

FDA Label Image

Hi (72189 158 90)

Label for Gabapentin 800 mg oral capsules by Direct Rx. The label indicates 90 tablets in the package and states Gabapentin as the generic ingredient. It includes lot and expiration dates along with packaging and distribution details. The label also references Neurontin as the original brand name.*

FDA Label Image

Hi (72189 113 90)

The label for Gabapentin 400 mg oral capsules contains 90 capsules. It is generic for Neurontin and shows each capsule contains 400 mg of Gabapentin. The label includes the lot number 24JN2001, expiration date 1/31/22, and states it is packaged and distributed by DirectRx in Dawsonville, GA. The label also features caution information and manufacturing details by Cap Labs Inc.*

FDA Label Image

Hi (72189 109 60)

The packaging label for Gabapentin 100 mg capsules by DIRECT RX features a yellow and white background with black text. It states 60 capsules per container and identifies Gabapentin as the generic equivalent of Neurontin. The label includes lot number, expiration date, and distribution details, along with additional smaller labels listing the same product information repetitively.*

FDA Label Image

Hi (72189 0178 90)

GABAPENTIN 800 mg oral capsules label from DIRECT RX showing a pack of 90 tablets. The label includes the NDC 72189-0178-90, generic reference to NEURONTIN, lot number 08FE2111, and expiration date 8/31/22. The packaging details manufacture information and caution statements regarding storage and use.*

FDA Label Image

Hi (72189 289 90)

Losartan Potassium and Hydrochlorothiazide (Losartan Pot/HCTZ) 100 mg / 25 mg oral film-coated tablets, 90 count, in a prescription label from DIRECT RX. The label includes NDC code 72189-289-90 and expiration date 01/31/25. The product is a generic form of Hyzaar.*

FDA Label Image

Hi (72189 109 30)

Gabapentin 100 mg oral capsules, 60 count, labeled as generic for Neurontin. Each capsule contains 100 mg of Gabapentin, distributed by Direct Rx. The label includes lot number, expiration date 10/31/21, and manufacturing information, with dosing instructions and FDA warnings partially visible.*

FDA Label Image

72189-158-60 (72189 158 60)

Gabapentin 800 mg oral capsules in a blister pack labeled with 60 tablets per package. The label indicates the product is a generic for Neurontin, containing 800 mg of gabapentin per coated tablet. Manufactured and packaged by Direct Rx.*

FDA Label Image

72189-178-30 (72189 178 30)

The packaging label for Gabapentin 800 mg capsules from Direct RX features a prominently displayed yellow and white design. It indicates that the package contains 30 tablets. The label states Gabapentin is generic for Neurontin and confirms each film-coated tablet contains 800 mg of gabapentin, USP. Additional details include the NDC number 72189-178-30 and manufacturing and expiration dates.*

FDA Label Image

72189-113-72 (72189 113 72)

The label for Gabapentin capsules, strength 400 mg, containing 120 capsules. It states Gabapentin as the generic form of Neurontin and specifies each capsule contains 400 mg USP Gabapentin. The label shows the NDC 72189-113-72 and indicates packaging and distribution by DIRECT RX in Dawsonville, GA. Additional text includes lot number, expiration date, and manufacturer details.*

FDA Label Image

72189-113-30 (72189 113 30)

Gabapentin 400 mg capsule bottle label from Direct Rx, containing 30 capsules. The label highlights that each capsule contains Gabapentin USP 400 mg and notes the generic equivalent to Neurontin. It includes dispensing, lot, and expiration information as sample data.*

FDA Label Image

72189-113-60 (72189 113 60)

Packaging label of Gabapentin 400 mg oral capsules by Direct Rx. The label indicates a bottle containing 60 capsules. It includes the product name Gabapentin with the generic reference to Neurontin. The label provides lot, sample, and expiration date information, along with directions to discard after a specified date. Manufacturer details note Caps Lab, Inc.*

* 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.