Buspirone Hydrochloride Tablet
Product Images NDC 72789-181

11 FDA label images from Pd-rx Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 72789-181). 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

10 mg ( Two Thirds Of A Tablet) (15mg 10mg)

10 mg ( Two Thirds Of A Tablet) (15mg 10mg)
An outlined illustration depicting two tablet halves, one marked with "0" and the other with "9", intended to demonstrate tablet splitting or scoring.*
FDA Label Image

15 mg (the Entire Tablet) (15mg 15mg)

15 mg (the Entire Tablet) (15mg 15mg)
Buspirone Hydrochloride 10 mg tablet with imprint code '093'. The tablet is scored and white, intended for oral administration. Manufactured by PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

5 mg (one Third Of A Tablet) (15mg 5mg)

5 mg (one Third Of A Tablet) (15mg 5mg)
Buspirone Hydrochloride 10 mg oral tablet packaging label from PD-Rx Pharmaceuticals, Inc. The image shows the tablet imprint marked with the number '0' on one side.*
FDA Label Image

7.5 Xxx (15mg 7 5)

7.5 Xxx (15mg 7 5)
Buspirone Hydrochloride 10 mg oral tablet shown partially in white with black printed text. The visible imprint includes a scoring line and the number '0'. The labeler is PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

10 mg (one Third Of A Tablet) (30mg 10mg)

10 mg (one Third Of A Tablet) (30mg 10mg)
The image shows a white tablet imprinted with the number 10 on one side. This is consistent with Buspirone Hydrochloride 10 mg oral tablets produced by PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

15 mg Entire Tablet (30mg 15mg)

15 mg Entire Tablet (30mg 15mg)
Buspirone Hydrochloride 10 mg oral tablet showing a scored white tablet with imprint "10 1" on one side. The tablet is manufactured by PD-Rx Pharmaceuticals, Inc. The image focuses on the tablet's imprint and partial scoring line.*
FDA Label Image

20 mg (two Thirds Of A Tablet) (30mg 20mg)

20 mg (two Thirds Of A Tablet) (30mg 20mg)
Buspirone Hydrochloride 10 mg oral tablet imprint showing '10' on both sides of a scored line, indicating the tablet strength and score line for splitting. The tablet is white and round, associated with PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

30 mg (the Entire Tablet) (30mg 30mg)

30 mg (the Entire Tablet) (30mg 30mg)
Buspirone Hydrochloride tablets, each scored and imprinted with the strength identifier '10' on all three segments, indicating 10 mg dosage. The white rectangular tablet is divided into three equal sections by score lines to facilitate breaking.*
FDA Label Image

Image (72789181)

Image (72789181)
Buspirone Hydrochloride USP 10 mg oral tablet label from PD-Rx Pharmaceuticals, Inc. The label indicates a 90 tablet count and includes warnings, dosage instructions, lot number F22E76, and expiration date 02/2024. The label features the NDC 72789-181-90, barcodes, and manufacturer information located in Oklahoma City, OK.*
FDA Label Image

Break In Half (Break)

Break In Half (Break)
An instructional illustration showing two hands holding a tablet, demonstrating how to split or break the tablet by applying pressure with the fingers at the scored line for oral administration.*
FDA Label Image

Structural Formula (Structural Formula)

Structural Formula (Structural Formula)
Chemical structure of buspirone hydrochloride depicting the molecular arrangement including cycloalkane and piperazine rings, attached functional groups, and hydrochloride salt representation.*

* 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.