Chlordiazepoxide Hydrochloride Capsule
Product Images NDC 70518-1752

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Chlordiazepoxide Hydrochloride (NDC 70518-1752). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

00555003302

Chlordiazepoxide Hydrochloride 10 mg oral capsule with a half black and half turquoise color. One side of the capsule is black with the imprint 'barr', and the other side is turquoise with the imprint '033'. No additional markings or packaging are visible.*

FDA Label Image

Mm1 (Remedy Label)

Chlordiazepoxide Hydrochloride 10 mg oral capsules label with a quantity of 30 capsules. The label identifies the drug as a Schedule IV controlled substance (C-IV) and states it is for prescription use only (RX ONLY). The manufacturer is listed as Teva, Frazer, PA. The label also includes storage instructions and notes the product is repackaged by RemedyRepack Inc., Indiana, PA.*

FDA Label Image

Chlordiazepoxide HCl 10mg 70518 1752 01

Chlordiazepoxide Hydrochloride 10 mg oral capsules, packaged in a quantity of 30. The label indicates Schedule IV (C-IV) controlled substance status and prescription-only (RX ONLY) use. Manufactured by Teva in Frazer, PA, and repackaged by RemedyRepack Inc., Indiana, PA. The label includes NDC 70518-1752-01 and instructions to see the package insert for use directions.*

FDA Label Image

Image 1

Chemical structure of Chlordiazepoxide Hydrochloride showing its molecular arrangement, including a chlorinated benzene ring and a benzodiazepine core with hydrochloride indicated.*

* 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.