Buspirone Hydrochloride Tablet
Product Images NDC 51655-511

4 FDA label images from Northwind Health Company, Llc · 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 51655-511). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Buspirone Structural Formula (Buspirone Str)

Buspirone Structural Formula (Buspirone Str)
Chemical structure of Buspirone Hydrochloride showing its molecular framework with labeled amide, piperazine, and pyrimidine rings, including the hydrochloride (HCl) component.*
FDA Label Image

Dosage Table (Buspirone Fig 1)

Dosage Table (Buspirone Fig 1)
Instructional chart showing how to break 15 mg or 30 mg tablets of Buspirone Hydrochloride to achieve various dosages. The left side illustrates breaking a 15 mg tablet into halves, thirds, and the full tablet for doses of 7.5 mg, 5 mg, 10 mg, and 15 mg. The right side shows similar breakage options for a 30 mg tablet to achieve doses of 8 mg, 10 mg, 15 mg, 20 mg, and 30 mg.*
FDA Label Image

Quadrisect Photo (Buspirone Fig 2)

Quadrisect Photo (Buspirone Fig 2)
Illustrations showing how to split Buspirone Hydrochloride tablets by hand. The first panel demonstrates splitting a 15 mg tablet, and the second panel shows splitting a 30 mg tablet. Each image depicts hands holding and breaking the tablet orally.*
FDA Label Image

Label (51655 511 52 Rev A 12 22 Nhc)

Label (51655 511 52   Rev A 12 22 Nhc)
Buspirone Hydrochloride 7.5 mg oral tablets packaging label from Northwind Health Company, LLC. The label indicates 30 tablets per container with instructions to store at controlled room temperature and keep out of reach of children. It includes the product's NDC 51655-511-52 and states 'Rx Only.'*

* 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.