Diethylpropion Hcl Controlled-release
Product Images NDC 68387-696

View Photos of 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 Diethylpropion Hcl Controlled-release (NDC 68387-696). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Keltman 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.

FDA Label Image

Label Image For 25mg (Tenuate 25mg)

Label Image For 25mg (Tenuate 25mg)
Diethylpropion HCl 25mg tablets label by Keltman Pharmaceuticals Inc., showing Generic Tenuate 25mg, 28 tablets per container. The label includes NDC 68387-695-28, lot number 079343 1, expiration date 1/2014, and prescription-only status. Instructions note storage below 30°C and caution about FDA reporting and prescription transfer restrictions.*
FDA Label Image

Label Image For 75mg Controlled Release (Tenuate 75mg)

Label Image For 75mg Controlled Release (Tenuate 75mg)
Diethylpropion HCl Controlled-Release 75 mg label from Keltman Pharmaceuticals Inc. The label states this product contains 28 tablets of Generic Tenuate 75 mg controlled release. It includes instructions for storage, cautionary notes, lot numbers, expiration date of 9/2013, and prescription information. The label also provides contact details to report side effects to the FDA.*
FDA Label Image

A9b96da2-figure-01 (A9b96da2 Figure 01)

A9b96da2-figure-01 (A9b96da2 Figure 01)
Chemical structure of diethylpropion hydrochloride, showing the molecular layout including a benzene ring, ketone group, and diethylamine moiety bonded to a hydrochloride component.*

* 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.