Temazepam Capsule
Product Images NDC 71205-915

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Temazepam (NDC 71205-915). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-914-30 (Temazepam 15mg 100s Count)

Label for Temazepam 15 mg oral capsules by Proficient Rx LP. The label indicates 30 capsules per package, mentions Temazepam USP 15 mg per capsule, and describes the capsule as having a blue opaque cap with "15 mg" imprint and white opaque body with "Novel 121" imprint. It includes regulatory markings such as RX Only and C-IV, the NDC 71205-914-30, and storage instructions.*

FDA Label Image

71205-915-30 (Temazepam 30mg 100s Count)

Label for Temazepam 30 mg capsules by Proficient Rx LP. The label indicates 30 capsules per bottle, prescription only, controlled substance schedule IV (C-IV). Each white opaque capsule is imprinted with "30 mg" on the cap and "Novel 123" on the body. Manufactured by Novel Laboratories Inc., Somerset, NJ.*

FDA Label Image

Temazepam (Temazepam Header)

Temazepam Capsules USP label showing the generic name temazepam and the Roman numeral IV symbol indicating Schedule IV controlled substance. The image presents the capsule dosage form for oral administration, as labeled by Proficient Rx LP.*

FDA Label Image

Temazepam-str (Temazepam Str)

Chemical structure diagram of temazepam, showing its molecular bonds and functional groups including a chlorine-substituted benzene ring, a lactam ring with a hydroxyl group, and a methylated nitrogen atom.*

* 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.