Oxcarbazepine Tablet, Film Coated
Product Images NDC 55154-4320

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 Oxcarbazepine (NDC 55154-4320). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, Llc, 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

Bag Label (4ebcb0e5 1c93 4b3f 8749 6835c56afce5 00)

Bag Label (4ebcb0e5 1c93 4b3f 8749 6835c56afce5 00)
This text contains information about OXCARBAZEPINE TABLETS, USP 300 mg. Each film-coated tablet contains 300 mg of oxcarbazepine. The usual dosage and complete prescribing information can be found in the product insert. Storage instructions indicate that the tablets should be stored at a temperature between 20°C - 25°C (77°F) with excursions permitted to 15°C - 30°C (59°F - 86°F). The medication contains FD&C Yellow No. 5 (tartrazine) as a color additive. The text also mentions that the packaging is not child resistant and is intended for institutional use only. The manufacturer is LGM Pharma Solutions, LLC, based in Irvine, CA. The distribution is handled by Breckenridge Pharmaceutical Inc. and Major Pharmaceuticals, with distribution by Cardinal Health.*
FDA Label Image

Bag Label (4ebcb0e5 1c93 4b3f 8749 6835c56afce5 01)

Bag Label (4ebcb0e5 1c93 4b3f 8749 6835c56afce5 01)
Oxcarbazepine Tablets, USP 150 mg is a medication that contains 10 film-coated tablets with each tablet containing 150 mg of oxcarbazepine. This medication is typically used to treat certain types of seizures in patients with epilepsy. The usual dosage and complete prescribing information can be found in the product insert. It is recommended to store the medication at a temperature between 20°C to 25°C (77°F) with excursions permitted to 15°C to 30°C (59°F to 86°F). The package includes an insert with additional medical guidance, which can be found at vww.majorpharmaceuticals.com. The medication contains FDAC Yellow No. 5 (tartarzine) as a color additive and is only available with a prescription. The unit dose packaging is not child resistant and is intended for institutional use only. It is essential to keep this and all drugs out of the reach of children and dispense them in a tight container. The medication is manufactured by LGM Pharma Solutions, LLC in Irvine, CA, and distributed by Brockenridge Pharmaceutical Inc in Berlin, CT. It is packaged and distributed by Major Pharmaceuticals in Indianapolis, IN, and distributed by Cardinal Health in Dublin, OH. Unfortunately, the provided text does not provide clear information on how to use the medication or possible side effects.*
FDA Label Image

Chemical Structure (Oxcarbazepine 01)

FDA Label Image

Figure 1 (Oxcarbazepine 02)

FDA Label Image

Figure 2 (Oxcarbazepine 03)

Figure 2 (Oxcarbazepine 03)
This text provides information about the seizure rate and statistical analysis related to a treatment group. The log-rank test was conducted, resulting in a p-value of 0.045. The table shows the days from the first dose to the first seizure for both the Oxcarbazepine and Placebo treatment groups.*
FDA Label Image

Figure 3 (Oxcarbazepine 04)

Figure 3 (Oxcarbazepine 04)
The text provided is not readable.*
FDA Label Image

Figure 4 (Oxcarbazepine 05)

Figure 4 (Oxcarbazepine 05)
This text appears to be a result from a statistical test, specifically a Tog-rank test. The given p-value is 0.0001. The text also includes a chart with a time scale labeled from 0 to 130, and a treatment group labeled as HIGH and LOW.*

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