Midodrine Hydrochloride Tablet
Product Images NDC 62332-338

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 62332-338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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

Midodrine 10 mg

Label for Midodrine Hydrochloride Tablets, USP 10 mg, containing 100 oral tablets. Manufactured by Alembic Pharmaceuticals Limited, India, for Alembic Pharmaceuticals, Inc., USA. Includes dosage unit strength, child-resistant package note, storage instructions, and barcode.*

FDA Label Image

Midodrine 2 5 mg

Label for Midodrine Hydrochloride Tablets, USP 2.5 mg, oral tablets. The package contains 100 tablets and is manufactured by Alembic Pharmaceuticals Inc. The label includes dosage strength, manufacturer details, storage instructions, and Rx only designation. The barcode and NDC 62332-338-31 are visible.*

FDA Label Image

Midodrine 5 mg

Label for Midodrine Hydrochloride Tablets, USP 5 mg by Alembic Pharmaceuticals Inc. The label shows a 100 tablet package intended for oral use. It includes storage instructions, a note that the package is child-resistant and sealed for protection, and manufacturer details from Alembic Pharmaceuticals Limited in India and Alembic Pharmaceuticals, Inc. in the USA. The NDC code 62332-339-31 and a barcode are also visible.*

FDA Label Image

Structure (Midodrine Structure)

Chemical structure diagram of Midodrine Hydrochloride showing its molecular components and arrangement with an HCl group indicated.*

* 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.