Paroxetine Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 63629-8527

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Paroxetine Hydrochloride (NDC 63629-8527). 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

Label (Lbl636298527)

This is a description of Paroxetine Hydrochloride extended-release tablets that contain 25 mg of paroxetine. It is important to keep this medication away from children, store it at a temperature of 20° to 25°C, and dispense it in a tight, light-resistant container with a child-resistant closure. The tablets should be swallowed whole and not broken, crushed, dissolved, or chewed. This description includes the NDC code, dosage form, and quantity of the medication, but does not provide any indications or recommended usage.*

FDA Label Image

Formula (Paroxetine Extended Release Tablets Usp 1)

FDA Label Image

Figure 1 (Paroxetine Extended Release Tablets Usp 2)

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Figure 2 (Paroxetine Extended Release Tablets Usp 3)

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Figure 3 (Paroxetine Extended Release Tablets Usp 4)

This text appears to be a chart or table with information on population description, including details on renal and hepatic impairment, age, gender, and pharmacokinetics. The chart includes dosing recommendations based on age and impairment level, as well as measurements of Cmax, AUC, and Cmin. The last two rows seem to show fold change and percent confidence intervals, with a value of 50.0 showing a relative change to the reference.*

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