Temazepam Capsule
Product Images NDC 43353-312

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Temazepam (NDC 43353-312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Temazepam (Temazepam Header)

Text panel titled 'Temazepam Capsules, USP' with the generic name temazepam and an indication of Schedule IV controlled substance status. The text includes the generic name in parentheses beneath the title.*

FDA Label Image

Temazepam-str (Temazepam Str)

Chemical structure of temazepam, showing its molecular framework with a chlorinated benzene ring, a methylated nitrogen, and a phenyl group attached to a diazepine ring with a hydroxyl and a ketone functional group.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Bottle Label 15 mg (43353 0312 10)

Temazepam 15 mg oral capsules packaging label displaying the product name, strength, and quantity (10 capsules). The label includes the NDC number 43353-0312-10, storage instructions, manufacturer Aphena Pharma Solutions - Tennessee, LLC in Somerset, NJ, and regulatory classifications including Schedule IV controlled substance information.*

FDA Label Image

Bottle Label 30 mg (43353 0260 60)

Packaging label for Temazepam 30 mg oral capsules by Aphena Pharma Solutions - Tennessee, LLC. The label indicates a package of 90 capsules with storage instructions between 20-25 degrees Celsius, and includes warnings, manufacturer and repackager details, NDC 43353-0260-60, and batch information.*

* 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.