Gabapentin
Product Images NDC 63629-7309

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 63629-7309). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

1 (Image 1)

1 (Image 1)
The given text is a formula to calculate the estimated creatinine clearance rate (cLcr) of a patient based on age, weight, and serum creatinine levels. It is commonly used in clinical settings to assess the kidney function of a patient. However, this formula alone cannot provide a definitive diagnosis and must be used in conjunction with other diagnostic tests.*
FDA Label Image

1 (Image 2)

FDA Label Image

1 (Image 3)

FDA Label Image

1 (Image 4)

FDA Label Image

1 (Image 5)

FDA Label Image

1 (Image 6)

1 (Image 6)
The text contains a chart with information about the mean pain score for a study that had a titration period of 4 weeks and a fixed dose period of 4 weeks. There were two groups in the study, one that received a placebo and another that received a maximum dose of 3600 mg/day of gabapentin. The chart shows the mean pain score at baseline and at weeks throughout the study.*
FDA Label Image

2 (Image 7)

2 (Image 7)
This text appears to be a chart or table with information regarding mean pain scores and treatment periods for different doses of gabapentin. Without additional context, its potential usefulness is limited.*
FDA Label Image

3 (Image 8)

FDA Label Image

4 (Image 9)

FDA Label Image

Label Image (Lbl636297309)

Label Image (Lbl636297309)
This text appears to be a medication label. The medication is called "Neurontin" and is a 400mg capsule produced by Watson Pharma Private Limited, with a package batch number of 07309901523487. The label includes information about storage instructions, expiration date, and the National Drug Code (NDC) number. The medication is listed as a controlled substance (CV).*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.