Midodrine Hydrochloride Tablet
Product Images NDC 51079-453

View Photos of 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 Midodrine Hydrochloride (NDC 51079-453). 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.

Product Images & Figures Index

FDA Label Image

Midodrine Hydrochloride Structural Formula (Image 01)

Midodrine Hydrochloride Structural Formula (Image 01)
Chemical structure of midodrine hydrochloride showing its molecular formula C12H18N2O4•HCl with a benzene ring substituted by hydroxymethyl, methoxy, and amidino groups.*
FDA Label Image

Midodrine Hydrochloride 5 mg Tablets Unit Carton Label (Image 02)

Midodrine Hydrochloride 5 mg Tablets Unit Carton Label (Image 02)
Midodrine Hydrochloride 5 mg oral tablets label from Mylan Institutional Inc. The label shows the product name, strength, dosage form, and NDC 51079-453-20. A round white tablet imprinted with 'MH' above '2' is shown. The packaging displays storage instructions and a barcode, indicating a package size of 100 tablets (10 x 10).*
FDA Label Image

Serialized Unit Carton (Image 03)

Serialized Unit Carton (Image 03)
Unit-dose packaging label for Midodrine Hydrochloride 5 mg tablets distributed by Mylan Institutional Inc. The blue label includes storage and handling warnings, highlights that the container is light-resistant, and shows a designated window for lot number and expiration date. The label is designed for institutional use and is not child resistant.*

* 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.