Midodrine Hydrochloride Tablet
Product Images NDC 70771-1595

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 70771-1595). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

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Chemical structure diagram of Midodrine hydrochloride, showing the molecular arrangement including a benzene ring with methoxy and hydroxymethyl groups and the hydrochloride salt component.*

FDA Label Image

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Midodrine Hydrochloride Tablets, USP 2.5 mg oral tablet label. The label shows the drug name prominently with strength 2.5 mg. It includes packaging details stating 100 tablets, Rx only, and manufacturer information for Zydus Lifesciences Limited. Additional text covers dosage strength per tablet and storage instructions.*

FDA Label Image

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Midodrine Hydrochloride Tablets, USP 5 mg oral tablets label showing 100 tablets per container. The label includes the NDC 70771-1596-1, manufacturer Zydus Lifesciences Limited, dosing information, storage instructions, and a depiction of a single round tablet embossed with '730'. The label also highlights prescription-only status and child-resistant packaging instructions.*

FDA Label Image

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Midodrine hydrochloride Tablets, USP 10 mg oral tablets shown on a pharmaceutical label. The label includes the product name, strength, quantity of 100 tablets, and manufacturer Cadila Healthcare Ltd., India. It instructs storage at 20° to 25°C and keeping the container tightly closed with child-resistant closure. The label also notes 'Rx only' and usual dosage directions refer to the package insert.*

* 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.