Losartan Potassium And Hydrochlorothiazide
Product Images NDC 50090-5295

3 FDA label images from A-s Medication Solutions · 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 50090-5295). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Structure01 (Image 1)

Structure01 (Image 1)
Chemical structure of Losartan Potassium, showing the molecular arrangement including a chlorinated pyrimidine ring, hydroxyethyl group, biphenyl moiety, and potassium ion (K+). This structure is consistent with the active ingredient in Losartan Potassium and Hydrochlorothiazide.*
FDA Label Image

Structure02 (Image 2)

Structure02 (Image 2)
Chemical structure of the active ingredient, Losartan Potassium, showing the molecular arrangement including a benzene ring with chlorine and sulfonamide groups, and a tetrazole moiety.*
FDA Label Image

Label Image (Lbl500905295)

Label Image (Lbl500905295)
Losartan Potassium and Hydrochlorothiazide 100 mg/12.5 mg tablets label from A-S Medication Solutions. The label shows a 30-tablet package with dosing instructions referencing a package insert. It includes storage instructions (25 to 70 degrees F) and manufacturer information including Teva Pharma Ltd. The image displays a white label on a brown bottle with printed text displaying NDC 50090-5295-0.*

* 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.