Brisdelle Capsule
Product Images NDC 83107-027

4 FDA label images from Legacy Pharma Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

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.

Product Images & Figures Index

FDA Label Image

Image Description (Brisdelle Caps Structure)

Image Description (Brisdelle Caps Structure)
Chemical structure diagram of paroxetine, the active ingredient in BRISDELLE 7.5 mg capsules. The structure shows the atoms and bonds typical for paroxetine's molecular composition.*
FDA Label Image
Image Description (Brisdelle Caps Logo)
FDA Label Image

Image Description (Brisdelle Caps 30s Blister Card)

Image Description (Brisdelle Caps 30s Blister Card)
Packaging label for BRISDELLE 7.5 mg capsules by Legacy Pharma USA, Inc. The label includes a dose calendar for 30 days, with individual day markers for tracking capsule intake. The design is simple with red outlines and purple highlight boxes denoting days for dosage and refill reminders.*
FDA Label Image

Image Description (Brisdelle Caps 30s Blister Carton)

Image Description (Brisdelle Caps 30s Blister Carton)
Packaging label for BRISDELLE (paroxetine) capsules, 7.5 mg per capsule, oral dosage form. The label indicates this is a prescription drug supplied by Legacy Pharma USA, Inc. The box contains 30 capsules. The label includes medication management instructions and child-resistant container opening directions, along with the NDC 83107-027-30 and website information www.Brisdelle.com.*

* 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.