Candesartan Cilexetil And Hydrochlorothiazide Tablet
Product Images NDC 70771-1325

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Candesartan Cilexetil And Hydrochlorothiazide (NDC 70771-1325). 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

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 03)

Label for Candesartan Cilexetil and Hydrochlorothiazide Tablets, USP, 16 mg/12.5 mg strength. The label shows an image of the tablet imprinted with '15 1', specifies a quantity of 1,000 tablets, listing Zydus Pharmaceuticals as the labeler and Cadila Healthcare Ltd, Ahmedabad, India as manufacturer. The NDC number 70771-1325-0 is displayed along with storage and dispensing instructions.*

FDA Label Image

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 04)

Label for Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 32 mg/12.5 mg strength. The label includes the NDC 70771-1326-0, shows images of two oval tablets with imprint 19 5, and states the package contains 1,000 tablets. It lists storage instructions and cautions to keep out of reach of children. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India, with Zydus Pharmaceuticals logo.*

FDA Label Image

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 05)

Label for candesartan cilexetil and hydrochlorothiazide tablets, USP, 32 mg/25 mg strength. The label includes the NDC number 70771-1327-0 and indicates packaging of 1,000 tablets. It shows an image of an oblong white tablet imprinted with '415'. The manufacturer is Cadila Healthcare Ltd., Ahmedabad, India, with Zydus Lifesciences Limited as the labeler. Storage and dispensing instructions are also present.*

* 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.