Clorazepate Dipotassium Tablet
Product Images NDC 70954-157

3 FDA label images from Ani 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 Clorazepate Dipotassium (NDC 70954-157). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani 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.

Product Images & Figures Index

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of clorazepate dipotassium showing the molecular arrangement including a chlorinated benzodiazepine core, a carboxylate group with potassium and potassium hydroxide components, and other key functional groups represented by standard chemical notation.*
FDA Label Image

Label1 (Clor Label 1)

Label1 (Clor Label 1)
Label for Clorazepate Dipotassium Tablets, USP, 3.75 mg strength, containing 100 tablets. The label includes dosing and storage instructions, manufacturer details (Novitium Pharma LLC), NDC 70954-159-10, and a barcode. The product is prescription-only and packaged in a light-resistant container.*
FDA Label Image

Label2 (Clor Label 2)

Label2 (Clor Label 2)
Clorazepate Dipotassium Tablets, USP, 7.5 mg, oral tablets packaged in a container of 100. The label shows the dosage strength prominently in green, includes storage instructions at 20° to 25°C, dispensing instructions, and the manufacturer as Novitium Pharma LLC, East Windsor, New Jersey. The label also provides the NDC number 70954-158-10 and instructs to dispense the enclosed medication guide to each patient.*

* 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.