Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 65862-468

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 65862-468). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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 (50 mg/12.5 mg (30 Tablet Bottle))

Label for Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg, film-coated tablets. The label states the product is Rx only, contains 30 tablets, and is distributed by Aurobindo Pharma USA, Inc. Storage instructions, dosage reference, and manufacturing origin (India) are also included. The label features the NDC 65862-468-30 and a barcode.*

FDA Label Image

Package Label-principal Display Panel (50 mg/12.5 mg Blister Carton (10 x 10 Unit-dose))

Packaging label for Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg, film-coated tablet form. The label shows a 100 tablet package (10 x 10 unit-dose) distributed by Aurobindo Pharma USA, Inc., with storage instructions and dosage advisory. The design includes the product name, strength, NDC 65862-468-10, and barcodes on multiple panels.*

FDA Label Image

Package Label-principal Display Panel (100 mg/12.5 mg (30 Tablet Bottle))

Packaging label for Losartan Potassium and Hydrochlorothiazide Tablets, USP, 100 mg/12.5 mg film-coated tablets by Aurobindo Pharma Limited. The label indicates 30 tablets per container, includes storage instructions, distributor information, and a barcode.*

FDA Label Image

Package Label-principal Display Panel (100 mg/12.5 mg Blister Carton (10 x 10 Unit-dose))

Packaging label for Losartan Potassium and Hydrochlorothiazide Tablets, USP, 100 mg/12.5 mg film-coated tablets. The label shows packaging for 100 tablets in 10 unit-dose packs. Distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions and dosage notes. NDC 65862-469-10.*

FDA Label Image

Package Label-principal Display Panel (100 mg/25 mg (30 Tablet Bottle))

Label of Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, film-coated, containing 30 tablets. Distributed by Aurobindo Pharma USA, Inc., made in India. Storage instructions and dosage information references included, along with barcode and NDC 65862-470-30.*

FDA Label Image

Package Label-principal Display Panel (100 mg/25 mg Blister Carton (10 x 10 Unit-dose))

Packaging label for Losartan Potassium and Hydrochlorothiazide Tablets, USP, 100 mg/25 mg film-coated tablets. The label indicates a package size of 100 tablets (10 x 10 unit-dose) and is distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions and states it is Rx only.*

FDA Label Image

Losartan Chemical Structure (Losartanhctz Str1)

Chemical structure diagram depicting the molecular arrangement of Losartan Potassium, illustrating its key atoms and bonds as part of the combination drug Losartan Potassium and Hydrochlorothiazide.*

FDA Label Image

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)

Chemical structure of losartan potassium and hydrochlorothiazide, showing the molecular arrangement including sulfonamide, chloro, and tetrazole groups as depicted in the structural formula diagram.*

* 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.