Buspirone Hydrochloride Tablet
Product Images NDC 71335-2820

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 71335-2820). 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

Structural Formula (3f939480 7edb 406e 896a C2055d0b09ea 01)

Chemical structure of Buspirone hydrochloride showing its molecular arrangement including a cyclopentane ring, piperazine ring, and pyrimidine ring with an attached hydrochloride group.*

FDA Label Image

Figure (3f939480 7edb 406e 896a C2055d0b09ea 02)

Illustration showing buspirone hydrochloride tablets with imprints 5 and ZE 38, and tablets with imprints 10 and ZE 39. The diagram indicates how to divide these tablets into fractional doses, including halves and thirds, corresponding to 7.5 mg, 15 mg, 20 mg, and 30 mg doses based on parts of 15 mg and 30 mg tablets.*

FDA Label Image

Figure (3f939480 7edb 406e 896a C2055d0b09ea 03)

Buspirone hydrochloride 7.5 mg oral tablet shown held between two fingers. The image focuses on the small, white scored tablet, emphasizing its size and shape suitable for oral administration.*

FDA Label Image

Label (Lbl713352820)

Buspirone hydrochloride 7.5 mg tablets label showing product name, strength, and dosage form. The label states the NDC number 71335-2820-1 and indicates 100 tablets per container. The labeler is Bryant Ranch Prepack, and the manufacturer is Zydus Lifesciences Ltd. It includes storage and dispensing instructions and features small QR codes and barcodes.*

* 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.