Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 65862-470

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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 65862-470). 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))

Package Label-principal Display Panel (50 mg/12.5 mg (30 Tablet Bottle))
This is a description of a prescription medication containing 50mg of Losartan Potassium USP and 125mg of Hydrochlorothiazide USP. It is a film-coated tablet distributed by Aurobindo Pharma USA, Inc. and is only available with a prescription. The usual adult dosage instructions are not readable in the provided text. The tablets must be stored at a controlled temperature of 20° to 25°C and kept tightly closed, away from light. The medication is made in India and has a specific product code. The NDC number is provided.*
FDA Label Image

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

Package Label-principal Display Panel (50 mg/12.5 mg Blister Carton (10 x 10 Unit-dose))
This is a description of Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg. The tablets are film-coated and each tablet contains 50 mg of Losartan potassium USP and 12.5 mg of hydrochlorothiazide USP. The usual adult dosage and storage instructions are provided. It also mentions that the unit-dose package is not child-resistant and a child-resistant container should be used. It is dispensed by Auraindo Pharma USA and the packaging contains 100 tablets. Made in India.*
FDA Label Image

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

FDA Label Image

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

Package Label-principal Display Panel (100 mg/12.5 mg Blister Carton (10 x 10 Unit-dose))
This is a product description for Losartan Potassium and Hydrochlorothiazide Tablets, USP, manufactured by Aurobindo Pharma USA. The tablets contain 100mg of losartan potassium and 12.5mg of hydrochlorothiazide. The recommended dosage for adults is not provided and must be referred to a circular that is presumably included. The tablets are to be stored in temperatures ranging from 20°C to 25°C and protected from light. The product is not child-resistant and a container approved for child-resistant packaging should be used if given for outpatient use. A lot code is provided: TSDRUGS 22009 for L. The National Drug Code (NDC) is 65862-469-10.*
FDA Label Image

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

Package Label-principal Display Panel (100 mg/25 mg (30 Tablet Bottle))
Losartan potassium and Hydrochlorothiazide Tablets, USP with strength of 100mg/25mg are distributed by Aurobindo Pharma USA Inc. The tablets are film-coated and come in a container of 30 tablets. The usual adult dosage information can be found in the accompanying circular. The tablets must be stored in USP controlled room temperature, and the container must be tightly closed and protected from light. The code for the product is TS/DRUGS/22/2009.*
FDA Label Image

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

Package Label-principal Display Panel (100 mg/25 mg Blister Carton (10 x 10 Unit-dose))
Losartan Potassium and Hydrochlorothiazide tablets are a medication used in adults to treat hypertension. Each tablet contains 100 mg of Losartan and 25 mg of hydrochlorothiazide. The usual adult dosage can be found in the accompanying circular. The tablets should be stored at a controlled room temperature of 20-25°C (68-77°F) and protected from light. The unit-dose package is not child-resistant, so a child-resistant container should be used if dispensed for outpatient use. The package contains 100 tablets in 10x10 unit-dose blisters. The manufacturer is Aurobindo Pharma, located at 270 Township Line Road, Suite 425, Blue Bell, PA, 19422.*
FDA Label Image

Losartan Chemical Structure (Losartanhctz Str1)

FDA Label Image

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)

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