Temazepam Capsule
Product Images NDC 50268-780

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Temazepam (NDC 50268-780). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

1 (779 15)

Label for temazepam capsules, USP 15 mg, manufactured by AvPAK. The label indicates the product is prescription only, containing 50 capsules in unit dose packaging (5 x 10). Storage instructions specify controlled room temperature, with warnings to keep out of reach of children. The label features the AvPAK logo and QR code.*

FDA Label Image

1 (780 13)

temazepam 30 mg capsules label for oral use, displaying the brand name and strength prominently with a red background for the strength. The package contains 30 capsules in unit dose format (6 x 5). The label includes dosing and storage information, manufacturer AvPAK details, a barcode, and a QR code. The label also indicates Rx only status and Controlled Substance Schedule IV classification.*

FDA Label Image

Temazepam (Temazepam Header)

A drug facts panel displaying the title 'Temazepam Capsules, USP' with the generic name 'temazepam' beneath it. It also includes a Roman numeral IV enclosed in a circle, indicating the drug's controlled substance schedule.*

FDA Label Image

Temazepam-str (Temazepam Str)

Chemical structure diagram of temazepam showing its molecular composition, including a benzodiazepine ring with chlorine, methyl, phenyl groups, and a carboxyl group.*

* 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.