Buspirone Hcl Tablet
Product Images NDC 72189-448

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hcl (NDC 72189-448). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

72189-448-90 (72189 0448 90)

Buspirone HCL 10 mg oral tablets packaging label showing a bottle with 90 tablets. The label indicates the product is a generic for Buspar, with each tablet containing 10 mg of Buspirone Hydrochloride USP. The label includes lot number SAMPLE, expiration date 10/31/24, and is packaged and distributed by Direct_Rx. The NDC is 72189-448-90.*

FDA Label Image

72189-448-60 (72189 448 60)

Buspirone HCL 10 mg oral tablet packaging label showing a quantity of 60 tablets. The label indicates Buspirone HCL as the active ingredient with the generic reference to Buspar. It also includes lot number 03AP2308 and a discard date of 09/30/24. The product is packaged and distributed by Direct Rx in Dawsonville, Georgia.*

FDA Label Image

72189-448-82 (72189 448 82)

Buspirone HCL 10 mg oral tablets, packaged as 180 count. The label states it is generic for Buspar and each tablet contains Buspirone Hydrochloride, USP 10 mg. Distributed by Direct Rx, with lot number 16MY2434 and expiration date 11/30/25. The label includes barcode and multiple references to manufacturing and NDC numbers.*

FDA Label Image

72189-448-30 (72189 448 30)

Buspirone HCL 10 mg oral tablet label shows a yellow and white design with the branded name Buspar. The label specifies a package of 30 tablets, each containing 10 mg of buspirone hydrochloride. The product is labeled by Direct Rx and includes lot number, expiration date, and manufacturing details. NDC 72189-448-30 is displayed at the top.*

* 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.