Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 0093-7367

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This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 0093-7367). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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.

FDA Label Image

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Losartan Potassium and Hydrochlorothiazide tablets are combination medications used for treating hypertension or high blood pressure. Each film coated tablet contains 50 mg of losartan potassium and 12.5 mg of hydrochlorothiazide. These tablets should be stored at controlled room temperature and should be kept in a tight-resistant container away from light. This medication should be dispensed only in a child-resistant closure as required. These tablets are manufactured in Israel by Teva Pharmaceutical Ind, Ltd and are manufactured for Teva Pharmaceuticals USA Inc, Parsippany. The usual dosage of the medication is mentioned in the package insert for full prescribing information.*
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This is a medication package of Losartan Potassium and Hydrochlorothiazide Tablets. Each film-coated tablet contains 100mg of Losartan Potassium and 12.5mg of Hydrochlorothiazide. It is used based on the dosage mentioned in the package insert for full prescribing information. The medication should be stored at 20° to 25°C (or 68° to 77°F) and kept away from light in a tightly closed container with a child-resistant closure. It is manufactured in Israel by Teva Pharmaceutical Ind. Ltd. and distributed by Teva Pharmaceuticals USA, Inc. The package contains 30 tablets and includes a Serialization Coding Area.*
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Losartan Potassium and Hydrochlorothiazide Tablets are a FDA approved prescription medicine used to treat high blood pressure (hypertension) in adults. Each film-coated tablet contains 100 mg losartan potassium, USP and 25 mg hydrochlorothiazide, USP. The medication should be stored at 20°to 25°C{68" o 77°F) and dispensed in a tight, resistant container as defined in the USP, witha child-resistant closure. The drug should be kept out of reach of children. The manufacturer is Teva Pharmacetical Ind, Ltd., Kfar Saba, 4410202, Isrzel and is Manufactured For. Teva Pharmaceticals USA, Inc., Parsippany, N) 07054. It is available in a pack of 30 tablets with NDC 0093-7368-56 and GTIN 00300937368564.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.