Phendimetrazine Tartrate Tablet
Product Images NDC 64850-440

3 FDA label images from Elite Laboratories, 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 Phendimetrazine Tartrate (NDC 64850-440). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elite Laboratories, 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

Phendimetrazine 35mg 1000ct

Phendimetrazine 35mg 1000ct
Label for Phendimetrazine Tartrate Tablets USP 35 mg by Elite Laboratories, Inc. The label states it contains 1000 oral tablets, prescription-only. It includes storage instructions, dosage reference to package insert, and a child-resistant container warning. The NDC is 64850-440-10. The label highlights the active ingredient phendimetrazine tartrate 35 mg per tablet and includes a barcode and manufacturer information.*
FDA Label Image

Phendimetrazine 35mg 100ct

Phendimetrazine 35mg 100ct
The image shows a label for Phendimetrazine Tartrate Tablets USP, 35 mg, oral tablet dosage form. It is manufactured by Elite Laboratories, Inc, Northvale, NJ. The label states the product is for prescription use only, sold in a container of 100 tablets. The NDC is 64850-440-01. Storage instructions include keeping the medication in a light-resistant container at 20° to 25°C.*
FDA Label Image

Phendimetrazine Tartrate Structure

Phendimetrazine Tartrate Structure
Chemical structure diagram showing the molecular formula C12H17NO·C4H6O6 and molecular weight 341.36, representing the active ingredient Phendimetrazine Tartrate.*

* 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.