Buspirone Hydrochloride Tablet
Product Images NDC 43063-785

4 FDA label images from Pd-rx Pharmaceuticals, 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 Buspirone Hydrochloride (NDC 43063-785). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

43063785 Label (43063785)

43063785 Label (43063785)
Label for Buspirone Hydrochloride 10 mg tablets, oral dosage form, containing 90 tablets. The label shows the product manufactured by PD-Rx Pharmaceuticals, Inc., with NDC 43063-785-90. Additional details include lot number D19D23 and expiration date 04/2021, along with warnings to keep out of reach of children and storage instructions.*
FDA Label Image

Dosage Table (Buspirone Fig 1)

Dosage Table (Buspirone Fig 1)
An instructional diagram showing dosing instructions for Buspirone Hydrochloride tablets, illustrating how to split 15 mg and 30 mg tablets into different doses (whole, two-thirds, one-third, and half) to achieve specific milligram amounts.*
FDA Label Image

Quadrisect Photo (Buspirone Fig 2)

Quadrisect Photo (Buspirone Fig 2)
An instructional illustration showing hands holding tablets labeled 'B M 4' and 'B 8', identified as 15 mg and 30 mg tablets respectively, demonstrating their size and identification markings.*
FDA Label Image

Buspirone Structural Formula (Buspirone Str)

Buspirone Structural Formula (Buspirone Str)
Chemical structure of Buspirone Hydrochloride showing its molecular composition including a piperazine ring and other characteristic functional groups.*

* 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.