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Levofloxacin Tablet, Film Coated
Product Images NDC 68180-241
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This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 68180-241). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lupin 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.
Product Images & Figures Index
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This is a drug prescription for Levofloxacin tablets, with a recommended adult dose provided separately. The tablets should be dispensed in a well-closed container and child-resistant container, and stored at a controlled room temperature. The tablets are manufactured by Lupin Pharmaceuticals in the USA and contain 0.250mg of Levofloxacin USP. The prescription includes 100 tablets and the NDC code is 68180-240-01.*
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This is a medication called Levofloxacin, which comes in the form of film-coated tablets. Each tablet contains 250 mg of anhydrous levofloxacin. It is a prescription drug and only available under the supervision of a doctor. The package includes 10 blister packs in each box, with 100 tablets in total. In case these tablets are given to an outpatient, a child-resistant container should be used as the bundle is not child-safe. It should be stored at controlled temperatures not exceeding 30°C (86°F) and at 15°C (59°F) at a minimum. The code of the drug is GO/DRUGS/654. The document includes the prescribing information required by pharmacists as well, and blisters should be retained within the box until usage time. The manufacturer of the package is Lupin Limited, which is based in Goa, India, and the drug is distributed by Lupin Pharmaceuticals in Baltimore, Maryland.*
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The text describes a medication labeled "ONCE-A-DAY" in a container with 100 tablets containing Levofloxacin. The medication guide must be dispensed separately by the pharmacist. The tablets are formulated with 500 mg anhydrous evofloacin hemiydrate USP, and the prescribing information should be consulted for the correct adult dose. The tablets must be dispensed in a well-closed container and stored at controlled room temperature. The manufacturer is Lupin Pharmaceuticals, Inc. based in Baltimore, Maryland, and Lupin Limited based in Goa, India. The code number is GODRUGS/S54 240438.*
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NDC 68180-241-13 Once-a-Day Levofloxacin Tablets USP are a medication for which the usual dosage should be consulted from the accompanying prescribing information. The tablets contain levofloxacin hemihydrate USP equivalent to 10500mg anhydrous levofloxacin. They are packaged in unit-dose blister packs; pharmacists are required to dispense a separate medication guide with each package. They should be stored at 25°C, with permitted excursions to 15°-30°C. The package is not child-resistant, and, if dispensed for outpatient use, a child-resistant container should be used. The lot number is indicated in the package.*
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This is a prescription drug labeled NDC 68180-242-01, manufactured by Lupin Pharmaceuticals. The medication, Levofloxacin, is available in the form of 750mg tablets and should be dispensed in a child-resistant container. The usual adult dose and prescribing information is provided separately. The code number is GO/DRUGS/B54. Store the tablets at a controlled room temperature.*
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The text is about Once-A-Day Levofloxacin Tablets USP manufactured and distributed by Lupin Limited and Lupin Pharmaceuticals. Each film-coated tablet contains levofloxacin hemihydrate USP equivalent to 750 mg anhydrous levofloxacin. The package is not child-resistant, and it is recommended to store at 25°C (77°F); excursions allowed to 15°-30°C (59°-86°F) per USP control room temperature guidelines. The package contains 100 (10x10) Rx only tablets. The text includes a code number of GO/DRUGS/654 as a reference.*
* 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.
