Buspirone Hydrochloride Tablet
Product Images NDC 71335-2073

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 71335-2073). 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 the tablet imprint codes and how to identify dosages of Buspirone Hydrochloride tablets. It details the front-side imprints for 30 mg tablets (B 3 0) and 15 mg tablets (B 1 5) and illustrates tablet divisions representing dosages of 10 mg, 15 mg, 20 mg (30 mg tablet fractions), and 5 mg, 7.5 mg, 10 mg (15 mg tablet fractions) based on halves and thirds of the whole tablet.*

FDA Label Image

Figure (Buspirone Fig2)

An illustration depicting hands holding a tablet, demonstrating splitting or breaking the tablet into two halves. This instructional diagram relates to the administration or handling of oral tablet dosage forms.*

FDA Label Image

Chemical Structure (Buspirone Str)

Chemical structure of buspirone hydrochloride, depicting its molecular arrangement with various ring systems and functional groups, including the hydrochloride (HCl) component.*

FDA Label Image

Label (Lbl713352073)

Label for Buspirone HCL 15 mg Tablet, packaged by Bryant Ranch Prepack in Burbank, CA. The label compares the product to Buspar 15 mg Tablet by Aurobindo Pharma Limited. It contains storage instructions and a barcode. The label also indicates a package size of 30 tablets and the product NDC 71335-2073-1.*

* 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.