Tramadol Hydrochloride And Acetaminophen
Product Images NDC 68387-497

3 FDA label images from Keltman 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 Tramadol Hydrochloride And Acetaminophen (NDC 68387-497). 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

37.5 mg/325 mg Label (Tramadol375label)

37.5 mg/325 mg Label (Tramadol375label)
Label for Tramadol Hydrochloride 37.5 mg and Acetaminophen 325 mg tablets by Keltman Pharmaceuticals, Inc. The package contains 120 tablets. It includes dosing information, lot number 007701, expiration date 4/2011, and states the product is Rx only. Manufacturer and distributor details are given, along with an FDA side effects reporting phone number.*
FDA Label Image

This Is Structure 1 (Str1)

This Is Structure 1 (Str1)
Chemical structure of the active ingredient in Tramadol Hydrochloride and Acetaminophen by Keltman Pharmaceuticals Inc., showing the molecular arrangement including a methoxy-substituted phenyl ring, cyclohexanol ring, and methylated amine group with associated hydrochloride.*
FDA Label Image

This Is Structure 2 (Str2)

This Is Structure 2 (Str2)
Chemical structure of Tramadol Hydrochloride and Acetaminophen, depicting the molecular arrangement with a hydroxyl group (OH) attached to a benzene ring and an amide functional group displayed.*

* 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.