Levofloxacin Tablet, Film Coated
Product Images NDC 67296-1104

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 67296-1104). 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

Package Label-principal Display Panel (250 mg (50 Tablet Bottle))

Package Label-principal Display Panel (250 mg (50 Tablet Bottle))
A packaging label for Levofloxacin Tablets USP, 250 mg, film-coated oral tablets. The label indicates a 50-tablet count and is labeled for once-a-day dosing. It notes distribution by Aurobindo Pharma USA, Inc., with manufacturing in India. The label includes storage instructions and a barcode on the right side.*
FDA Label Image

Package Label-principal Display Panel (250 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (250 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Levofloxacin Tablets USP 250 mg oral film-coated tablets. The label indicates a prescription drug with once-a-day dosing and contains 100 unit-dose tablets (10 x 10). Distributed by Aurobindo Pharma USA, Inc., the product is made in India. The label includes storage instructions, pharmacist warnings, and a barcode.*
FDA Label Image

Package Label-principal Display Panel (500 mg (50 Tablet Bottle))

Package Label-principal Display Panel (500 mg (50 Tablet Bottle))
Levofloxacin Tablets USP 500 mg film-coated oral tablets label for once-a-day prescription use. The label includes dosage instructions, pharmacy dispensing information, storage conditions (20° to 25°C), and manufacturer details showing Aurobindo Pharma USA, Inc. Distribution, with the product made in India. The package contains 50 tablets and has barcodes and NDC 65862-537-50.*
FDA Label Image

Package Label-principal Display Panel (500 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (500 mg Blister Carton (10 x 10 Unit-dose))
Label packaging for Levofloxacin Tablets USP 500 mg oral film-coated tablets. The label indicates a once-a-day dosage with 100 unit-dose tablets per container. Distributed by Aurobindo Pharma USA, the label includes storage instructions, pharmacy dispensing information, and manufacturer details. The design features purple text highlights and the Aurobindo logo.*
FDA Label Image

Package Label-principal Display Panel (750 mg (20 Tablet Bottle))

Package Label-principal Display Panel (750 mg (20 Tablet Bottle))
Label for Levofloxacin Tablets USP 750 mg, film-coated tablets for oral use. The label states 'Once-a-day' dosing and includes 20 tablets per container. It is distributed by Aurobindo Pharma USA, Inc., with manufacturing in India. The label includes storage instructions and a barcode.*
FDA Label Image

Package Label-principal Display Panel (750 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (750 mg Blister Carton (10 x 10 Unit-dose))
Carton label for Levofloxacin Tablets USP 750 mg film-coated tablets for oral use. The label indicates a 100 count unit-dose tablet package, distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions, dispensing information, and the barcode. The manufacturer Aurobindo Pharma is noted, although the labeler data says Redpharm Drug.*
FDA Label Image

Chemical Structure (Levofloxacin Str)

Chemical Structure (Levofloxacin Str)
Chemical structure of levofloxacin depicting its molecular components including fluorine, oxygen, nitrogen atoms, and associated hydrogen bonding with half a molecule of water (1/2 H2O).*

* 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.