Oxcarbazepine Suspension
Product Images NDC 69452-125

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Oxcarbazepine (NDC 69452-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Carton (Carton)

Carton (Carton)
This is a description of Oxcarbazepine, an oral suspension medication. It is distributed by Bionpharma in Princeton. It must be shaken before use and used within 7 weeks of first opening. It is important to dispense a medication guide to each patient. Each 5 mL contains 300 mg of Oxcarbazepine, USP. The medication must be stored below 30°C and kept away from children. Dosage information is available in the package insert.*
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Structural Formula (Image01)

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Image 5 (Image010)

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Image 6 (Image011v2)

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Image 7 (Image012v2)

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Image 8 (Image013v2)

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Image 9 (Image014v2)

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Image 10 (Image015v2)

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Figure 1 (Image02)

Figure 1 (Image02)
This appears to be a table with three columns. The third column contains two groups, "Oxcarbazeping" and "Placebo", likely for a study or clinical trial. The first column has a header that reads "Log-rarkcres", though it is unclear what this refers to. The second column may have to do with the timing of measurements or observations, as it contains a "Time on Tl fom Dy (8ays)" header. Beyond this, the text is not very clear.*
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Figure 2 (Image03)

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Figure 3 (Image04)

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Figure 4 (Image05)

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Image 1 (Image06)

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Image 2 (Image07v2)

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Image 3 (Image08)

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Image 4 (Image09)

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Image Description (Revisedimage016)

Image Description (Revisedimage016)
BIONPHARMA manufactures an oral suspension medication called Oxcarbazepine. The medication is packed in a bottle of 250 ml and its NDC is 69452-125-50. Pharmacists are advised to dispense a Medication Guide enclosed with the medication to each patient. It is important to shake the bottle well before using. The medication should be used within 7 weeks of first opening the bottle. The label suggests that this is a prescription-only medication manufactured by BIONPHARMA located in Princeton, NJ 08540.*

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