Buspirone Hydrochloride Tablet
Product Images NDC 72189-175

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 72189-175). 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

17530 (72189 0175 30)

Buspirone HCL 10 mg tablet bottle label by Direct RX. The label states the product name Buspirone HCL with strength 10 mg and contains 30 tablets. It identifies the generic name Buspar and mentions each tablet contains Buspirone Hydrochloride USP 10 mg. The label includes lot, product, and expiry details, as well as packaging information and manufacturer location in Dawsonville, GA.*

FDA Label Image

20 (72189 200 82)

BUSPIRONE HYDROCHLORIDE 10 mg oral tablets packaged in a bottle containing 180 tablets. The label shows the product name BUSPIRONE HCL with strength 10 mg and package size 180 tablets. It is labeled for generic substitution for BUSPAR. The labeler is DIRECT RX with lot and expiration dates visible, along with the NDC number 72189-200-82.*

FDA Label Image

72189-175-90 (72189 175 90)

Packaging label for Buspirone HCL 10 mg oral tablets, containing 90 tablets per container. The label indicates the product is generic for Buspar, with each tablet containing Buspirone Hydrochloride USP 10 mg. Manufactured and distributed by DIRECT Rx, with lot number 04MA2109, expiration date 10/31/22, and packaging location Dawsonville, GA.*

FDA Label Image

72189-175-82 (72189 175 82)

Packaging label for Buspirone HCL 10 mg oral tablets, containing 180 tablets per bottle. The label indicates Buspirone Hydrochloride USP 10 mg per tablet, generic for Buspar. The labeler is DIRECT RX, with lot number 26AP2416 and expiration date 02/28/2025. Additional manufacturing and NDC information is present in smaller text.*

* 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.