Chlordiazepoxide Hydrochloride
Product Images NDC 67296-1491

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Chlordiazepoxide Hydrochloride (NDC 67296-1491). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug 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

Chlordiazepoxide Hydrochloride Structural Formula (Images 1)

Chemical structure of Chlordiazepoxide Hydrochloride, showing the molecular arrangement of its atoms including a chlorinated benzodiazepine core and hydrochloride (HCl) component.*

FDA Label Image

1 (Images 2)

Packaging label for Chlordiazepoxide Hydrochloride Capsules USP 5 mg. The label indicates a quantity of 100 capsules. It includes storage instructions, warnings about child safety, and a pharmacist dispensing note. The label features the Teva Pharmaceuticals name and logo and contains a space labeled Serialization Coding Area. The NDC shown is 0555-0158-02.*

FDA Label Image

1 (Images 3)

Chlordiazepoxide Hydrochloride Capsules USP 10 mg label showing a 100-capsule package by Teva Pharmaceuticals USA Inc. The label includes dosage information, storage instructions, and an NDC (0555-0033-02). It specifies pharmacist dispensing instructions and a warning to keep out of reach of children.*

FDA Label Image

1 (Images 4)

Chlordiazepoxide Hydrochloride Capsules USP 25 mg by Teva Pharmaceuticals USA, shown on a label indicating 100 capsules per bottle. The label includes directions for storage, dispensing instructions, an NDC number (0555-0159-02), and warnings to keep out of reach of children. The label design features green and white colors with the Teva logo.*

* 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.