Buspirone Hydrochloride Tablet
Product Images NDC 70518-2987

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Buspirone Hydrochloride (NDC 70518-2987). 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

Remedy_label (Remedy Label)

The description of the product is as follows: busPIRone HCI is a 15mg tablet manufactured by Oxford Pharmaceuticals in Birmingham, AL. The NDC # is 70518-2987-00 and it is repackaged by Remedy Repack Inc. with a quantity of 30 tablets per bottle. The lot number and expiration date are not available. The product should be kept out of the reach of children and stored at 20-26°C (63-77°F) with permissible excursions to 15-30°C (59-86°F). Directions for use can be found in the package insert. This is a prescription-only medication.*

FDA Label Image

Mm2 (Buspirone HCl 15mg 70518 2987 01)

This is a description of a medication named busPIRone HCI, which has a 15mg strength and comes in a tablet form. The medication is manufactured by Oxford Pharmaceuticals in Birmingham, AL 3211. The package contains 60 tablets and its National Drug Code (NDC) is 70518-2987-01. The lot number is not given. The source NDC is 69584-0093-50. The medication should be stored at a temperature between 20-26°C (63-77°F), with excursions permitted to 15-30°C (59-86°F). There are no usage instructions provided, except to refer to the package insert. The packaging has been repackaged by RemedyRepack Inc. and is RX only.*

FDA Label Image

Structural Formula (Structural Formula)

* 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.