Benzphetamine Hydrochloride
Product Images NDC 53217-175

3 FDA label images from Aidarex Pharmaceuticals 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 Benzphetamine Hydrochloride (NDC 53217-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

B2f154cc-figure-01 (Benzphetamine HCl 1)

B2f154cc-figure-01 (Benzphetamine HCl 1)
Chemical structure of Benzphetamine Hydrochloride showing its molecular formula C17H21N with molecular weight 275.82. The diagram depicts the arrangement of atoms and bonds in the compound associated with Aidarex Pharmaceuticals LLC product.*
FDA Label Image

B2f154cc-figure-02 (Benzphetamine HCl 2)

B2f154cc-figure-02 (Benzphetamine HCl 2)
A data table presenting Body Mass Index (BMI) values expressed in kg/m2. The table correlates BMI with different weights (pounds) in rows and heights (feet, inches) in columns, showing BMI values for various combinations of height and weight.*
FDA Label Image

Package Label (Benzphetamine HCl 3)

Package Label (Benzphetamine HCl 3)
Packaging label for Benzphetamine Hydrochloride 50 mg tablets by Aidarex Pharmaceuticals LLC. The label states generic for Didrex, quantity 90 tablets, NDC 53217-0175-90. The tablet is described as a peach round tablet with BP 650 on one side and a score on the reverse. Manufacturer is Boca Pharmaceutical, L.L.C., Coral Springs, FL. Additional prescription and caution information, plus Rx numbers, appear on the right side.*

* 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.