Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 62332-050

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 62332-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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.

FDA Label Image

Losartanhctz 50 125 mg

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP containing 50 mg of Losartan potassium and 12.5 mg of Hydrochlorothiazide per film-coated tablet. The label indicates a 30-tablet count, prescription-only status, and includes storage instructions and manufacturer information from Alembic Pharmaceuticals Inc. It also features a note for the pharmacist to dispense with the patient information leaflet.*

FDA Label Image

Losartanhctz Hctz

Chemical structure diagram of the active ingredient Losartan Potassium and Hydrochlorothiazide, showing molecular components including benzene rings and sulfonamide groups.*

FDA Label Image

Losartanhctz Losar

Chemical structure diagram of Losartan Potassium, the active ingredient in Losartan Potassium and Hydrochlorothiazide tablets. The structure shows the molecular arrangement including potassium (K+) ion.*

FDA Label Image

Losartanhctz mg 100 125

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/12.5 mg strength, film-coated oral tablets. The label indicates a package quantity of 30 tablets, prescription use only, and is manufactured by Alembic Pharmaceuticals Inc. Storage instructions and dosage warnings are also present, along with a barcode and NDC 62332-049-30.*

FDA Label Image

Losartanhctz mg 100 25

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP 100 mg/25 mg, film-coated oral tablets. The label indicates a package of 30 tablets by Alembic Pharmaceuticals, with storage instructions and a barcode. The label includes dosage details and states 'Rx only'.*

* 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.