Midodrine Hydrochloride Tablet
Product Images NDC 60687-398

10 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 60687-398). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

10 mg Midodrine HCl Tablet Blister

10 mg Midodrine HCl Tablet Blister
Midodrine Hydrochloride 10 mg oral tablet packaging label from American Health Packaging, Columbus, OH. The label includes the drug name, strength, lot number 123456, and expiry date 07/18. Multiple identical labels are shown in a vertical layout with barcode and expiration details.*
FDA Label Image

10 mg Midodrine HCl Tablet Carton

10 mg Midodrine HCl Tablet Carton
Label for Midodrine Hydrochloride Tablets, USP, 10 mg strength by American Health Packaging. The label indicates 30 tablets per container and includes an NDC number 60687-409-25. Storage instructions and safety warnings about keeping the product out of reach of children and handling the blister correctly are included on the label.*
FDA Label Image

2.5 mg Midodrine HCl Tablet Blister.jpg

2.5 mg Midodrine HCl Tablet Blister.jpg
Midodrine Hydrochloride Tablet, USP 2.5 mg tablet labels arranged in a grid. Each label includes the product name, strength, a barcode, section for lot number and expiration date, and American Health Packaging information. The labels are white with black text.*
FDA Label Image

2.5 mg Midodrine HCl Tablets Carton.jpg

2.5 mg Midodrine HCl Tablets Carton.jpg
Label for Midodrine Hydrochloride Tablets, USP, 2.5 mg strength. The label shows the product name, dosage form as tablets, and packaging of 100 tablets (10 x 10). It is labeled for oral use and prescription only, with storage instructions and drug protection information. The labeler is American Health Packaging.*
FDA Label Image

5 mg Blister

5 mg Blister
Midodrine Hydrochloride 5 mg tablets labels from American Health Packaging. Each label displays the drug name, strength (5 mg), route (oral), lot number (1234567), and expiry date (02/22). The labels include barcodes and are arranged in a sheet format for printing or packaging use.*
FDA Label Image

5 mg Carton

5 mg Carton
Midodrine Hydrochloride 5 mg oral tablets label from American Health Packaging. The label shows the dosage strength as 5 mg and indicates a package size of 100 tablets (10 by 10). It includes storage instructions, a warning to keep out of reach of children, and directs users to the package insert for dosage information. NDC 60687-398-01 is visible.*
FDA Label Image

Atx13200

Atx13200
Midodrine Hydrochloride 2.5 mg oral tablet imprinted with 'APO' on one side and 'MID 2.5' on the other. The round white tablet is used for prescription use and labeled by American Health Packaging.*
FDA Label Image

Atx13210

Atx13210
Midodrine Hydrochloride 5 mg oral tablet imprinted with 'APO' on one side and 'MID' over '5' on the other. The pink, round tablets are labeled by American Health Packaging as prescription medicine for oral use.*
FDA Label Image

Atx13250

Atx13250
Midodrine Hydrochloride 10 mg round blue oral tablet imprinted with 'APO' on one side and 'MID 10' on the other. The tablet is a prescription drug labeled by American Health Packaging.*
FDA Label Image

Structural Formula

Structural Formula
Chemical structure of Midodrine Hydrochloride showing its molecular arrangement including methoxy and hydroxyl groups attached to the aromatic ring along with the hydrochloride component 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.