Midodrine Hydrochloride Tablet
Product Images NDC 59651-247

7 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 59651-247). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Fig1 (Midodrine Fig1)

Fig1 (Midodrine Fig1)
Label for Midodrine Hydrochloride Tablets USP 2.5 mg by Aurobindo Pharma Limited. The label includes the NDC 59651-246-01, active ingredient Midodrine Hydrochloride USP 2.5 mg per tablet, along with inactive ingredients. It states the product is prescription-only and provides storage instructions. The package contains 100 tablets and is distributed by Aurobindo Pharma USA, Inc.*
FDA Label Image

Fig2 (Midodrine Fig2)

Fig2 (Midodrine Fig2)
Packaging label for Midodrine Hydrochloride Tablets, USP 2.5 mg, an oral prescription drug by Aurobindo Pharma Limited. The label displays the product name, strength, quantity (100 tablets), and NDC 59651-246-01. It includes active ingredient and inactive ingredients information, storage instructions, and distributor details: Aurobindo Pharma USA, Inc., East Windsor, NJ. The label also shows barcodes and the product is made in India.*
FDA Label Image

Package Label-principal Display Panel (5 mg (100 Tablets Bottle))

Package Label-principal Display Panel (5 mg (100 Tablets Bottle))
Label for Midodrine Hydrochloride Tablets USP 5 mg oral tablets, distributed by Aurobindo Pharma USA, Inc. The label includes the NDC 59651-247-01 and states the package contains 100 tablets. Active ingredient is Midodrine Hydrochloride USP 5 mg per tablet. The label lists inactive ingredients, storage instructions, and distributor contact information. A barcode and a coding area are also visible.*
FDA Label Image

Package Label-principal Display Panel (5 mg (100 Tablets Carton))

Package Label-principal Display Panel (5 mg (100 Tablets Carton))
Packaging label for Midodrine Hydrochloride Tablets, USP 5 mg, oral tablets by Aurobindo Pharma Limited. The label indicates 100 tablets per package, Rx only. It includes active ingredient details, inactive ingredients, storage instructions, and distributor information for Aurobindo Pharma USA, Inc. with barcode and NDC 59651-247-01 visible.*
FDA Label Image

Package Label-principal Display Panel (10 mg (100 Tablets Bottle))

Package Label-principal Display Panel (10 mg (100 Tablets Bottle))
Midodrine Hydrochloride Tablets, USP 10 mg carton label from Aurobindo Pharma Limited. Contains 100 tablets. The label shows active ingredient Midodrine Hydrochloride USP 10 mg per tablet and lists inactive ingredients. Distributed by Aurobindo Pharma USA with address in New Jersey. Storage instructions and coding area are also visible along with an NDC number and barcode.*
FDA Label Image

Package Label-principal Display Panel (10 mg (100 Tablets Carton))

Package Label-principal Display Panel (10 mg (100 Tablets Carton))
Packaging label for Midodrine Hydrochloride Tablets, USP 10 mg by Aurobindo Pharma Limited. The carton indicates 100 tablets, prescription use only, with active ingredient Midodrine Hydrochloride USP 10 mg per tablet. It includes storage instructions and mentions inactive ingredients. Distributed by Aurobindo Pharma USA, Inc., made in India, featuring a barcode and NDC 59651-248-01.*
FDA Label Image

Chemical Structure (Midodrine Str)

Chemical Structure (Midodrine Str)
Chemical structure of Midodrine Hydrochloride showing its molecular components, including a benzene ring with methoxy and hydroxymethyl substituents, an amide group, and a hydrochloride component (HCl).*

* 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.