Moxifloxacin Tablet, Film Coated
Product Images NDC 81033-068

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 81033-068). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corportation, 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

Chemical Structure (Structure)

Chemical structure of moxifloxacin hydrochloride, the active ingredient in Moxifloxacin 400 mg film-coated tablets by Kesin Pharma Corporation. The diagram shows the molecular configuration including fluorine, oxygen, nitrogen, and hydrochloride groups.*

FDA Label Image

Plasma Figure (Plasmacurve)

A line graph showing plasma concentration (µg/mL) of a drug over time (hours) following oral and intravenous (i.v.) administration. The y-axis represents plasma concentration, peaking shortly after dosing, and the x-axis represents time up to 28 hours. Two curves compare oral dose (circles) and i.v. dose (squares), both declining over time.*

FDA Label Image

Kesin Pharma Logo (Kesin Logo)

FDA Label Image

Moxifloxacin Tablets 400 mg 30 Count Carton (Moxifloxacintabs 400mg Carton 30ct)

Moxifloxacin Tablets, USP 400 mg film-coated tablets packaging label from Kesin Pharma Corporation. The label specifies 30 tablets in a unit dose format (3 x 10). The packaging is marked Rx Only and includes a pharmacist instruction to dispense the accompanying Medication Guide to each patient. The product NDC is 81033-068-31.*

FDA Label Image

Moxifloxacin Tablets 400 mg 50 Count Carton (Moxifloxacintabs 400mg Carton 50ct)

Packaging label for Moxifloxacin Tablets, USP 400 mg film-coated oral tablets by Kesin Pharma Corporation. The carton holds 50 tablets in 5 unit dose blister packs of 10 tablets each. The label features prescription status, NDC 81033-068-51, pharmacist dispensing instructions, and storage information.*

* 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.