Levofloxacin Tablet, Film Coated
Product Images NDC 67296-2126

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 67296-2126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Structure Product Formula For Levofloxacin (1e751b41 167b 4844 A3a6 Ff1a84ec0cad 01)

Chemical structure of levofloxacin monohydrate, showing its molecular framework and the associated 1/2 H2O molecule.*

FDA Label Image

Levofloxacin Tablets, 250 mg (1e751b41 167b 4844 A3a6 Ff1a84ec0cad 02)

Label for Levofloxacin Tablets USP 250 mg by Viona Pharmaceuticals. The label indicates 50 film-coated oral tablets, prescription only, with instructions for pharmacists to dispense the Medication Guide. Storage and dosage instructions, manufacturer (Zydus Lifesciences Ltd.) and distributor details are included.*

FDA Label Image

Levofloxacin Tablets, 500 mg (1e751b41 167b 4844 A3a6 Ff1a84ec0cad 03)

Levofloxacin Tablets, USP 500 mg film-coated oral tablets packaging label. The label indicates once-a-day dosing, contains 50 tablets, and is prescription only. It is manufactured by Viona Pharmaceuticals Inc. and includes storage and medication guide instructions. The NDC on the label is 72578-099-18.*

FDA Label Image

Levofloxacin Tablets, 750 mg (1e751b41 167b 4844 A3a6 Ff1a84ec0cad 04)

Levofloxacin Tablets, USP 750 mg film-coated tablets, bottle label for 20 tablets. The label states once-a-day dosing, pharmacist dispensing instructions, pharmacy and distributor information including manufacturer Zyidus Lifesciences Ltd., India, and distributor Viona Pharmaceuticals Inc., NJ. Storage instructions and child-resistant packaging information are also included. The NDC displayed is 72578-100-92.*

* 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.