Buspirone Hydrochloride Tablet
Product Images NDC 82804-039

View Photos of 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 Buspirone Hydrochloride (NDC 82804-039). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Patient Instruction Sheet (Buspirone Fig1)

Patient Instruction Sheet (Buspirone Fig1)
An instructional diagram depicting dosage markings for buspirone hydrochloride tablets. It shows tablet imprint details for 30 mg and 15 mg strengths, identifying how to split tablets into halves or thirds with corresponding partial doses labeled. Front side imprints include "B30" for 30 mg and "B15" for 15 mg tablets, with no markings on the other side.*
FDA Label Image

Figure (Buspirone Fig2)

Figure (Buspirone Fig2)
An illustration showing a pair of hands breaking a tablet in half. The image demonstrates how to split a tablet, likely for dosing purposes.*
FDA Label Image

82804-039-60 (Buspirone Fig5)

82804-039-60 (Buspirone Fig5)
Label for Buspirone HCl 7.5 mg tablets with 60 count, labeled by Proficient Rx LP. Tablets are described as white, ovoid rectangular, beveled edge, uncoated, debossed with "B" and "75" separated by a score line on one side. Manufactured by Aurobindo Pharma Limited, India. Storage instructions indicate 20° to 25°C.*
FDA Label Image

Chemical Structure (Buspirone Str)

Chemical Structure (Buspirone Str)
Chemical structure diagram of buspirone hydrochloride, showing its molecular components including rings and functional groups labeled with atoms and bonds.*

* 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.