Gabapentin Capsule
Product Images NDC 71205-532

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 71205-532). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-532-30 (223a9216 6e07 49b9 8faf Bb4e529a6ae5 00)

Gabapentin 300mg capsules, NDC 71205-532-90, are packaged by Proficient RX LP in Thousand Oaks, CA. The capsules are white to off-white powder-filled, size 1 hard gelatin capsules with an opaque yellow-colored cap and body. The capsules have SG imprinted on the cap and 180 on the body with black ink. A medication guide must be provided to each patient when dispensing the capsules. It is a prescription drug and should be kept out of the reach of children. The lot number for this product is 00000, and it should be stored at 20°-25°C (68°-77°F) with an expiry date of 00/00/00.*

FDA Label Image

Chemical Structure (Gabapentin 01)

FDA Label Image

Figure 1 (Gabapentin 02)

This is a report related to pain management that shows the mean pain score after the administration of O-piscebo and Gabapertin (at a dosage of 3600 mg/day) over a period of 12 weeks. The baseline pain score is also provided for comparison purposes.*

FDA Label Image

Figure 2 (Gabapentin 03)

The text is a table showing the medication regime of Gabapentin for pain management over the course of several weeks. The pain score is also noted throughout this period.*

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Figure 3 (Gabapentin 04)

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Figure 4 (Gabapentin 05)

* 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.