Buspirone Hydrochloride Tablet
Product Images NDC 70518-0380

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 70518-0380). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

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Chemical structure diagram of buspirone hydrochloride showing its molecular framework including a piperazine ring, a cyclopentane moiety, and associated functional groups with the hydrochloride salt indicated.*

FDA Label Image

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An instructional diagram showing different portions and sides of Buspirone hydrochloride 15 mg and 30 mg tablets for dosage reference. It visually breaks down whole tablets into halves, thirds, and two-thirds, with imprint codes 5 and ZE 38 on the 15 mg tablets, and 10 and ZE 39 on the 30 mg tablets to help identify and dose the medication correctly.*

FDA Label Image

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Buspirone hydrochloride 15 mg oral tablet shown held between two fingers. The tablet is white, oblong, and scored. No additional markings or packaging are visible in the image.*

FDA Label Image

Remedy_label (Remedy Label)

Buspirone hydrochloride 15 mg tablet label showing quantity of 30 tablets. The label includes Rx only designation, NDC number 70518-0380-00, manufacturer Zydus Pharm, and repackager RemedyRepack Inc. Packaging includes storage instructions and advises to see package insert for directions. The label features RemedyRepack logo and a barcode.*

* 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.