Chlordiazepoxide Hydrochloride Capsule
Product Images NDC 58118-1033

3 FDA label images from Clinical Solutions Wholesale, Llc · 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 Chlordiazepoxide Hydrochloride (NDC 58118-1033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, 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

00555003302

00555003302
Chlordiazepoxide Hydrochloride 10 mg capsule, oval-shaped with one half black and the other half light blue-green. One side is imprinted with 'barr' and '033' in white. The capsule is for oral use and labeled by Clinical Solutions Wholesale, LLC.*
FDA Label Image

Chlordiazepoxide 10mg

Chlordiazepoxide 10mg
Label for Chlordiazepoxide Hydrochloride 10 mg Capsules by Clinical Solutions Wholesale, showing NDC 58118-1033-8 and a quantity of 30 capsules. The label includes manufacturer information for Teva Pharmaceuticals USA Inc, North Wales, PA, USA, and repackager information for Clinical Solutions Wholesale, LLC in Franklin, TN. Additional details include lot number SAMPLE123 and batch number SAMPLE4567.*
FDA Label Image

Chlordiazepoxide Hydrochloride Structural Formula (Chlordiazepoxide Hydrochloride Capsule 1)

Chlordiazepoxide Hydrochloride Structural Formula (Chlordiazepoxide Hydrochloride Capsule 1)
Chemical structure diagram of the active ingredient Chlordiazepoxide Hydrochloride, showing the molecular arrangement including a chlorinated benzene ring and a diazepine ring, with an attached hydrochloride component.*

* 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.