Losartan Potassium And Hydrochlorothiazide
Product Images NDC 50090-4301

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 50090-4301). 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.

Product Images & Figures Index

FDA Label Image

Label Image (Lbl500904301)

Label Image (Lbl500904301)
Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg tablet bottle label from A-S Medication Solutions. The bottle contains 90 tablets. The label includes lot number, storage instructions to protect tablets from light, and packaging/manufacturer information including Aurbindo Pharma Limited and NDC 50090-4301-0.*
FDA Label Image

Losartan Chemical Structure (Losartanhctz Str1)

Losartan Chemical Structure (Losartanhctz Str1)
Chemical structure of the active ingredients Losartan Potassium and Hydrochlorothiazide, showing the molecular arrangement of both components with potassium ion indicated.*
FDA Label Image

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)

Hydrochlorothiazide Chemical Structure (Losartanhctz Str2)
Chemical structure diagram showing the molecular structure of the active ingredients losartan potassium and hydrochlorothiazide. The diagram includes a chlorobenzene ring, sulfonamide group, and tetrazole ring characteristic of losartan potassium, as well as the sulfonamide and chloride functional groups related to hydrochlorothiazide.*

* 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.