Midodrine Hydrochloride Tablet
Product Images NDC 46708-338

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 46708-338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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

100 Tablets (Midodrine 10mg)

Label for Midodrine Hydrochloride Tablets, USP 10 mg, an oral tablet containing midodrine hydrochloride, manufactured by Alembic Pharmaceuticals Limited. The package contains 100 tablets and includes storage instructions, child-resistant packaging notice, NDC 46708-340-31, and a barcode.*

FDA Label Image

100 Tablets (Midodrine 25mg)

Midodrine Hydrochloride Tablets, USP 2.5 mg oral tablets packaging label from Alembic Pharmaceuticals Limited. The label states the product contains 100 tablets, prescription only, with storage instructions, child-resistant packaging, and manufacturer details from Gujarat, India. NDC 46708-338-31 is visible.*

FDA Label Image

100 Tablets (Midodrine 5mg)

Label for Midodrine Hydrochloride Tablets, USP 5 mg oral tablets by Alembic Pharmaceuticals Limited. The label shows the NDC 46708-339-31 and indicates a package of 100 tablets. Storage instructions include maintaining 25°C with permitted excursions. The label mentions child-resistant packaging and directs users to the package insert for dosage information.*

FDA Label Image

Structure (Midodrine Structure)

Chemical structure of Midodrine Hydrochloride showing its molecular arrangement with functional groups including hydroxyl, amine, methoxy, and amide attached to a benzene ring, along with the hydrochloride salt form 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.