Spironolactone And Hydrochlorothiazide Tablet
Product Images NDC 42292-017

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Spironolactone And Hydrochlorothiazide (NDC 42292-017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional Inc., 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

Spironolactone Structural Formula (Image 01)

Chemical structure of spironolactone, one of the active ingredients in Spironolactone and Hydrochlorothiazide tablets by Mylan Institutional Inc. The structure shows the steroid backbone with specific functional groups including ketones, a sulfur atom, and acetyl groups.*

FDA Label Image

Hydrochlorothiazide Structural Formula (Image 02)

Chemical structure diagram depicting the molecular arrangement of the active ingredient spironolactone and hydrochlorothiazide.*

FDA Label Image

Spironolactone & Hydrochlorothiazide 25 mg/25 mg Tablets Unit Carton Label (Image 03)

The label for Spironolactone and Hydrochlorothiazide Tablets USP shows a strength of 25 mg / 25 mg. It displays the round tablet imprint 'M 41' and is labeled for prescription use only. The packaging is for a bottle containing 100 tablets, and the product is manufactured by Mylan Pharmaceuticals Inc.*

FDA Label Image

Serialized Unit Carton (Image 04)

Unit-dose packaging for Spironolactone and Hydrochlorothiazide tablets from Mylan Institutional Inc. The blue package features institutional-use warnings, safety instructions about child reach and light resistance, the Mylan logo, and a window for lot number and expiration date. No strength or dosage details are visible on this packaging image.*

* 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.