Buspirone Hydrochloride Tablet
Product Images NDC 50268-135

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 50268-135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

15 (135 15 15mg)

Label for Buspirone Hydrochloride Tablets, USP, 15 mg oral tablets. The label indicates Rx only, 50 tablets in unit dose packaging (5 x 10). It includes a barcode, storage instructions at 20° to 25°C, and manufacturer information for AvPAK, Pulaski, TN. The label also states to keep out of reach of children and to dispense with a patient instructions sheet.*

FDA Label Image

Structural Formula (2a7745f5 4376 4a0a B040 Fdd441205d8d 01)

Chemical structure of buspirone hydrochloride, depicting the molecular arrangement of atoms including the cyclohexane ring, piperazine ring, pyrimidinyl group, and the hydrochloride component.*

FDA Label Image

Figure (2a7745f5 4376 4a0a B040 Fdd441205d8d 02)

An instructional diagram showing the partial tablet dosing options for Buspirone hydrochloride tablets in 15 mg and 30 mg strengths. It illustrates how to divide each tablet into halves, thirds, or two thirds to achieve various doses, depicting tablet segments labeled with numerical values and identifiers such as '5', '10', 'ZE 38', and 'ZE 39' corresponding to each dose fraction.*

FDA Label Image

Figure (2a7745f5 4376 4a0a B040 Fdd441205d8d 03)

A black-and-white image showing two hands holding a single tablet of buspirone hydrochloride approximately between their thumb and forefinger, demonstrating the tablet size and shape for oral administration.*

* 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.