Gabapentin Tablet, Film Coated
Product Images NDC 72789-127

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 72789-127). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 01)

The text seems to be a medical formula likely used to calculate creatinine clearance (CLCr) in a patient based on their serum creatinine levels and weight. The calculation may need to be modified by multiplying by 0.35 for female patients. However, without more context it's hard to say for certain.*

FDA Label Image

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 02)

FDA Label Image

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 03)

This text appears to be a chart or graph with information on a pain study that includes a 4-week dose titration period and a 4-week fixed dose period with a placebo and Gabapentin dosage of 3600 mg/day. The chart also includes a baseline and a mean pain score of 10. Without additional context or further information, it is difficult to provide a more detailed description.*

FDA Label Image

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 04)

FDA Label Image

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 05)

This appears to be a chart showing percentages and monetary values related to a study. However, without further context, it is not possible to give a useful description.*

FDA Label Image

Gabapentin Tablets (49957454 Bd5a 4d3c 85cf 6fe78aa2c11e 06)

FDA Label Image

72789127 Label (72789127)

This is a description of a medication called Gabapentin. The medication comes in a bottle containing 90 film-coated tablets each of 600 mg strength. The medication may cause drowsiness, and individuals taking it should avoid alcohol to prevent impairment while driving vehicles or operating other heavy machinery. The tablets should be taken three times a day. The medication has a lot number of 120E68, was manufactured by PD-Rx Pharmaceuticals in Oklahoma City, and has an expiration date of 11/2021.*

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