Buspirone Hydrochloride Tablet
Product Images NDC 71335-2081

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 71335-2081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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)

An instructional diagram showing tablet imprint codes and corresponding doses for buspirone hydrochloride tablets in 30 mg and 15 mg strengths. It illustrates the front and other side markings for whole tablets and fractions (half, two thirds, one third) to indicate varying doses from 7.5 mg up to 30 mg.*

FDA Label Image

Figure (Buspirone Fig2)

An instructional illustration showing two hands splitting or breaking a tablet. The image demonstrates how to properly hold and break the tablet into halves using the thumbs and fingers.*

FDA Label Image

Chemical Structure (Buspirone Str)

Chemical structure of buspirone hydrochloride showing its molecular arrangement with a bicyclic ring, piperazine ring, and an aromatic ring with nitrogen atoms, including the hydrochloride component.*

FDA Label Image

Label (Lbl713352081)

Label for Buspirone Hcl 10 mg Tablet, a human prescription drug packaged by Bryant Ranch Prepack in Burbank, CA. The label compares this product to Buspar 10 mg Tablet by Aurobindo Pharma Limited. It includes storage instructions, a barcode, lot number, and states the package contains 30 tablets with NDC 71335-2081.*

* 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.