Losartan Potassium And Hydrochlorothiazide
Product Images NDC 50090-5141

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 50090-5141). 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

Image (C5a05595 80eb 44af A812 52beb290793e 01)

Image (C5a05595 80eb 44af A812 52beb290793e 01)
Chemical structure of Losartan Potassium, showing the molecular arrangement including chlorine, hydroxyl, and phenyl groups along with the potassium ion (K+). No other product components are depicted.*
FDA Label Image

Image (C5a05595 80eb 44af A812 52beb290793e 02)

Image (C5a05595 80eb 44af A812 52beb290793e 02)
Chemical structure of the active ingredient in Losartan Potassium and Hydrochlorothiazide, showing its molecular framework including nitrogen, sulfur, oxygen, chlorine, and carbon atoms arranged in a distinctive ring system.*
FDA Label Image

Label Image (Lbl500905141)

Label Image (Lbl500905141)
Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg film-coated tablets in a 90-tablet bottle. The label indicates the product contains Losartan Potassium USP (amorphous) and Hydrochlorothiazide USP, each 50 mg and 12.5 mg respectively, manufactured by A-S Medication Solutions, with product NDC 50090-5141-0. Storage instructions specify protecting from light and storing at 77 degrees Fahrenheit.*

* 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.