Gabapentin Tablet, Film Coated
Product Images NDC 72162-2141
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Gabapentin (NDC 72162-2141). 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.
Product Images & Figures Index
Chem Structure (D45f499b 8612 479e 8dd2 4fe28b1f5f9c 01)
Figure01 (D45f499b 8612 479e 8dd2 4fe28b1f5f9c 02)
Figure02 (D45f499b 8612 479e 8dd2 4fe28b1f5f9c 03)
Figure03 (D45f499b 8612 479e 8dd2 4fe28b1f5f9c 04)
Figure4 (D45f499b 8612 479e 8dd2 4fe28b1f5f9c 05)
Label (Lbl721622141)
Gabapentin Tablets, USP 600 mg is a medication that is available in film-coated tablet form. Each tablet contains 600 mg of Gabapentin. It should be stored at a temperature of 20° to 25°C (68° to 77°F), with excursions allowed between 15° to 30°C (59° to 86°F). The tablets should be dispensed in a tight, light-resistant container with a child-resistant closure. It is important to keep this medication out of the reach of children. Each patient should be provided with a Medication Guide. The NDC (National Drug Code) for this product is 72162-2141-1. The tablets are manufactured by ACI Healthcare Limited and relabeled by Bryant Ranch Prepack, Inc. This medication is available in a package containing 100 tablets.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.