Phendimetrazine Tartrate
Product Images NDC 52959-886

3 FDA label images from H.j. Harkins Company, 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 52959-886). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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

C:\documents And Settings\avyas\desktop\phend-outsert\spl\phendimetrazine-image-a.jpg (3e594fab Figure 01)

C:\documents And Settings\avyas\desktop\phend-outsert\spl\phendimetrazine-image-a.jpg (3e594fab Figure 01)
Chemical structure diagram of Phendimetrazine Tartrate, showing its molecular configuration with labeled atoms and bonds.*
FDA Label Image

3e594fab-figure-04 (3e594fab Figure 04)

3e594fab-figure-04 (3e594fab Figure 04)
PHENDIMETRAZINE TARTRATE ER 35 mg tablet packaging label from H.J. Harkins Company, Inc. The label shows the product name, strength, dosage form, lot number PHZ00KV, manufacturer KVK-TECH in Newtown, PA, and expiration date 10/12. It compares to Bontril with NDC 10702-077-10. The label includes usage instructions to follow the doctor's directions and displays multiple small labels for 42 count bottles.*
FDA Label Image

52959 0886 Ppac Label

52959 0886 Ppac Label
Label for PHENDIMETRAZINE TARTRATE ER 105mg capsules, displaying manufacturer Sandoz and labeler H.J. Harkins Company, Inc. Features include NDC 52959-0886-XX, lot number AB00CD, expiration 00/00, caution about federal law and prescription requirements, and multiple barcode sections. The label also mentions the product is comparable to Bontril SR.*

* 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.