Losartan Potassium Tablet, Film Coated
Product Images NDC 65841-731

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 65841-731). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Losapotataba (628ca159 4668 4f76 9c62 B541e59416ae 06)

Label for Losartan Potassium Tablets, USP 25 mg oral film-coated tablets by Zydus Lifesciences Limited. The label shows 100 tablets per container with instructions to keep out of children’s reach. It includes storage conditions and manufacturer details by Cadila Healthcare Ltd., India. The NDC is 65841-729-01.*

FDA Label Image

Losapotatabb (628ca159 4668 4f76 9c62 B541e59416ae 07)

Losartan Potassium Tablets, USP 50 mg film-coated oral tablets, labeled for prescription use only. Package contains 100 tablets. Label includes dosage strength, manufacturer Zydus Lifesciences Limited, and NDC 65841-730-01. The label also features a barcode and safety instructions regarding storage and child protection.*

FDA Label Image

Losapotatabc (628ca159 4668 4f76 9c62 B541e59416ae 08)

Label for Losartan Potassium Tablets, USP 100 mg film-coated tablets. The label shows a white oval tablet imprinted with 'Z 18'. It contains 100 tablets and is for prescription use only. The labeler is Zydus Lifesciences Limited, manufactured by Cadila Healthcare Ltd., India. The label includes handling instructions and dosage directions in small text.*

* 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.