Losartan Potassium And Hydrochlorothiazide
Product Images NDC 68071-1947

3 FDA label images from Nucare Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 68071-1947). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (68071 1947 3 A138)

Pdp (68071 1947 3 A138)
Packaging label for Losartan Potassium and Hydrochlorothiazide tablets, 100 mg/12.5 mg strength, by NuCare Pharmaceuticals, Inc. The label indicates 30 film-coated tablets per package, with an oval white shape debossed with 'F' on one side and '74' on the other. The label includes lot number, expiration date, NDC 68071-1947-3, and storage instructions at controlled temperature 68-77°F.*
FDA Label Image

Losartan Chemical Structure (Losartanhctz Str1)

Losartan Chemical Structure (Losartanhctz Str1)
Chemical structure of losartan potassium, depicting the molecular arrangement of its atoms and bonds, including the potassium ion (K+). This image relates to the active ingredient in Losartan Potassium and Hydrochlorothiazide by NuCare Pharmaceuticals, Inc.*
FDA Label Image

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)
Chemical structure diagram of the active ingredient Losartan Potassium and Hydrochlorothiazide, showing the molecular bonds and specific functional groups characteristic of this compound.*

* 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.