Midodrine Hydrochloride Tablet
Product Images NDC 0245-0213

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midodrine Hydrochloride (NDC 0245-0213). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, Llc, 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

Principal Display Panel (2.5 mg Tablet Bottle Label)

Label for Midodrine Hydrochloride Tablets, USP 2.5 mg oral tablets, containing 100 tablets per package. The label shows the NDC number 0245-0211-11, manufacturer Upsher-Smith Laboratories, LLC, Maple Grove, MN, and dosage information with storage instructions. It is marked Rx only and includes a barcode.*

FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Label for Midodrine Hydrochloride Tablets USP 5 mg, oral tablet form, supplied in a package of 100 tablets. The label includes storage instructions and manufacturer information, identifying Upsher-Smith Laboratories, LLC as the labeler. It states the product is prescription only and sealed for protection.*

FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Label for Midodrine Hydrochloride Tablets USP, 10 mg, manufactured by Upsher-Smith Laboratories, LLC. The label indicates a package of 100 oral tablets, prescription only, with storage instructions and barcode. The label emphasizes the 10 mg strength and includes manufacturer details.*

FDA Label Image

Chemical Structure (Midodrine HCl Tab 01)

Chemical structure of midodrine hydrochloride showing its molecular arrangement with hydroxyl, amide, and methoxy functional groups attached to a benzene ring and an associated hydrochloride moiety.*

* 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.