Temazepam Capsule
Product Images NDC 68788-8081

3 FDA label images from Preferred Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Temazepam (NDC 68788-8081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Temazepam Cap Usp 30mg Civ (Temazepam 30mg 100s Count)

Temazepam Cap Usp 30mg Civ (Temazepam 30mg 100s Count)
Label for Temazepam Cap USP 30mg capsules by Preferred Pharmaceuticals Inc. The label identifies the product as a generic for Restoril with each capsule containing 30 mg of temazepam. The label includes storage instructions, caution about federally prohibited drug transfer, dosage instructions in English and Spanish, and manufacturer information for Ascend Laboratories, LLC. Several fields for lot number, expiration date, and product number are present but blank.*
FDA Label Image

Temazepam (Temazepam Header)

Temazepam (Temazepam Header)
Temazepam Capsules USP 30 mg oral capsules. The label shows the proprietary and generic name temazepam with the strength of 30 mg. The label also displays the Roman numeral IV, indicating schedule IV controlled substance classification. Manufactured by Preferred Pharmaceuticals Inc.*
FDA Label Image

Temazepam-str (Temazepam Str)

Temazepam-str (Temazepam Str)
Chemical structure of temazepam, showing a fused benzodiazepine ring with chlorine substitution, a methylated nitrogen, a phenyl group, and a hydroxyl group attached to the core structure.*

* 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.