Benzphetamine Hydrochloride
Product Images NDC 75834-100

3 FDA label images from Nivagen 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 Benzphetamine Hydrochloride (NDC 75834-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nivagen 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

Chemical Structure (Benzphetamine 01)

Chemical Structure (Benzphetamine 01)
Chemical structure diagram of Benzphetamine Hydrochloride showing its molecular arrangement with phenyl groups and hydrochloride component, corresponding to the active ingredient Benzphetamine Hydrochloride by Nivagen Pharmaceuticals, Inc.*
FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

Principal Display Panel (50 mg Tablet Bottle Label)
Label for Benzphetamine Hydrochloride Tablets 50 mg, Rx only, containing 30 tablets. The label includes the NDC 75834-102-30 and states the usual adult dosage, pharmacist instructions, and storage conditions. It is distributed by Nivagen Pharmaceuticals, Inc. and manufactured by Tedor Pharma Inc. The label also includes a barcode and standard warnings.*
FDA Label Image

Principal Display Panel (25 mg Tablet Bottle Label)

Principal Display Panel (25 mg Tablet Bottle Label)
Label for Benzphetamine Hydrochloride Tablets 25 mg by Nivagen Pharmaceuticals, Inc. The label indicates Rx only and a count of 30 tablets. It includes dosage instructions, storage conditions, a warning to keep out of reach of children, distribution and manufacturing details, and a barcode.*

* 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.