Levofloxacin
Product Images NDC 21695-041

6 FDA label images from Rebel Distributors Corp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 21695-041). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Levofloxacin Structural Formula (F82ee9e3 5119 4be0 883c 5831386baef6 01)

Levofloxacin Structural Formula (F82ee9e3 5119 4be0 883c 5831386baef6 01)
Chemical structure of levofloxacin, showing its molecular arrangement including a fluorine atom, piperazine ring, carboxyl group, and other functional groups. The structure also indicates the presence of half a molecule of water (1/2 H2O) as a hydrate component.*
FDA Label Image

Figure 2: Mean Levofloxacin Plasma Concentration Vs. Time Profile: 750 mg (F82ee9e3 5119 4be0 883c 5831386baef6 02)

Figure 2: Mean Levofloxacin Plasma Concentration Vs. Time Profile: 750 mg (F82ee9e3 5119 4be0 883c 5831386baef6 02)
A pharmacokinetic line graph showing plasma concentration (mcg/mL) over time (hours) for Levofloxacin 750 mg administered as a tablet orally and as an intravenous infusion over 90 minutes. The chart compares plasma concentration changes for both administration routes up to 36 hours.*
FDA Label Image

Figure 3: Mean Levofloxacin Plasma Concentration Vs. Time Profile: 500 mg (F82ee9e3 5119 4be0 883c 5831386baef6 03)

Figure 3: Mean Levofloxacin Plasma Concentration Vs. Time Profile: 500 mg (F82ee9e3 5119 4be0 883c 5831386baef6 03)
A line graph comparing plasma concentration (mcg/mL) of 500 mg Levofloxacin over time (hours) for oral (p.o.) tablet and intravenous (i.v.) administration. The x-axis represents time in hours, and the y-axis shows plasma concentration in micrograms per milliliter, illustrating drug concentration decline post-dose.*
FDA Label Image

Levofloxacin 250mg (F82ee9e3 5119 4be0 883c 5831386baef6 04)

Levofloxacin 250mg (F82ee9e3 5119 4be0 883c 5831386baef6 04)
Levofloxacin 250 mg tablets label from Physician Partner, containing 10 tablets for once-a-day dosage. The label states each tablet contains 250 mg Levofloxacin and describes the tablets as terra cotta pink, film-coated, oval-shaped, debossed with TEVA on one side and 7291 on the other. The manufacturer is Teva Pharmaceuticals Ind. LTD, Jerusalem, Israel. Storage instructions specify controlled room temperature 15°-30°C (59°-86°F).*
FDA Label Image

Levofloxacin 500mg (F82ee9e3 5119 4be0 883c 5831386baef6 05)

Levofloxacin 500mg (F82ee9e3 5119 4be0 883c 5831386baef6 05)
Levofloxacin 500mg tablets container label from Physician Partner. The label indicates 10 tablets, once-a-day dosage, with active ingredient strength 500mg per tablet. Tablets are described as peach-colored, film-coated, oval-shaped bearing debossed markings 'TEVA' and '7292'. The label shows packaging and shipping information by Physician Partner, Thousand Oaks, CA, with storage instructions at controlled room temperature 15°-30°C (59°-86°F). Manufacturer is Teva Pharmaceuticals Ind. LTD., Jerusalem, Israel.*
FDA Label Image

Levofloxacin 750mg (F82ee9e3 5119 4be0 883c 5831386baef6 06)

Levofloxacin 750mg (F82ee9e3 5119 4be0 883c 5831386baef6 06)
Label for Levofloxacin 750 mg tablets, 10 count, once-a-day dosage form. The label indicates the product is prescription only (RX Only) and includes details such as the NDC number 21695-041-10, product ID PL004110, and manufacturer Teva Pharmaceutical Industries Ltd., Jerusalem, Israel. The label is from Physician Partner, Thousand Oaks, CA, and includes storage instructions and warnings.*

* 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.