Midodrine Hydrochloride Tablet
Product Images NDC 72603-606

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 72603-606). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Midodrine Hydrochloride Tablets, Usp 10mg (100 Tablets)

Label for Midodrine Hydrochloride Tablets USP 10 mg by NorthStar Rx LLC. The label states the product contains 100 tablets, with storage instructions between 20° to 25°C and child-resistant packaging. Manufactured by Rubicon Research Ltd., India, the label includes warnings to keep medication out of children's reach and references accompanying prescribing information.*

FDA Label Image

Midodrine Hydrochloride Tablets, Usp 2.5mg (100 Tablets)

Label for Midodrine Hydrochloride Tablets, USP 2.5 mg, oral tablets in a bottle of 100 tablets. The label includes dosage strength, storage instructions, and manufacturer information. The product is labeled as Rx Only and manufactured for NorthStar Rx LLC, with manufacturing by Rubicon Research Ltd.*

FDA Label Image

Midodrine Hydrochloride Tablets, Usp 5mg (100 Tablets)

Label for Midodrine Hydrochloride Tablets USP 5 mg, showing a 100-tablet supply. The label includes dosage form as oral tablets, manufacturer information for Northstar Rx LLC and Rubicon Research Ltd., and storage instructions. It emphasizes child-resistant packaging and safe storage temperatures.*

FDA Label Image

Structure (Midodrine Hydrochloride Tab Structure 01)

Chemical structure of Midodrine Hydrochloride depicted as a 2D molecular diagram illustrating its atomic groups and bonding.*

* 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.