Brisdelle Capsule
Product Images NDC 83107-027

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Brisdelle (NDC 83107-027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Legacy Pharma Usa, 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

Image Description (Paroxetine Caps 30s Blister Card)

Brisdelle (paroxetine) Capsules 7.5 mg per capsule packaging label by Sebela Pharmaceuticals, Inc. The label indicates an oral capsule dosage form with 30 capsules per container. It includes child-resistant container opening instructions, helpful medication information, and the NDC 54766-907-53 labeler code. The label is primarily purple and white, with the website Brisdelle.com noted for more information.*

FDA Label Image

Image Description (Paroxetine Caps 30s Blister Carton)

Packaging label for BRISDELLE 7.5 mg capsules (paroxetine) by Legacy Pharma USA, Inc. The label features a 30-day blister pack layout with daily dosage markings from Day 1 to Day 30. The capsules are organized in rows with some capsules shown in purple. The label includes a barcode and space for the starting date.*

FDA Label Image

Image Description (Paroxetine Caps Logo)

FDA Label Image

Image Description (Paroxetine Caps Structure)

Chemical structure diagram showing the molecular formula of the active ingredient paroxetine. The diagram includes multiple rings and functional groups consistent with the paroxetine molecule, as used in the drug BRISDELLE 7.5 mg oral capsules by Legacy Pharma USA, Inc.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.