Skip to the page

Data / Drug companies / Midodrine hydrochloride

Midodrine hydrochloride: 34 companies and 109 products in the FDA NDC directory

Midodrine hydrochloride is listed in the FDA National Drug Code Directory by 34 companies, with 109 products in commercial distribution. 109 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on September 1, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
34
Products
109
Generic (ANDA) products
109 (100.0%)
Application numbers
12
Routes
Oral
openFDA record search
api.fda.gov

Companies that list midodrine hydrochloride

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack7tabletGeneric drugs (ANDA)October 15, 2020
Major Pharmaceuticals6tabletGeneric drugs (ANDA)September 1, 2026
NorthStar RxLLC6tabletGeneric drugs (ANDA)June 15, 2026
Bryant Ranch Prepack4tabletGeneric drugs (ANDA)August 10, 2020
Bryant Ranch Prepack4tabletGeneric drugs (ANDA)October 15, 2020
Cardinal Health 107, LLC4tabletGeneric drugs (ANDA)September 12, 2006
Advagen Pharma Ltd3tabletGeneric drugs (ANDA)August 19, 2019
Alembic Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)January 22, 2021
Alembic Pharmaceuticals Limited3tabletGeneric drugs (ANDA)January 22, 2021
American Health Packaging3tabletGeneric drugs (ANDA)June 6, 2019
Apotex Corp.3tabletGeneric drugs (ANDA)September 12, 2006
Aurobindo Pharma Limited3tabletGeneric drugs (ANDA)August 10, 2020
AvKARE3tabletGeneric drugs (ANDA)May 5, 2017
AvPAK3tabletGeneric drugs (ANDA)August 26, 2019
First Nation Group, LLC3tabletGeneric drugs (ANDA)August 13, 2025
Golden State Medical Supply, Inc.3tabletGeneric drugs (ANDA)October 1, 2020
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)March 25, 2026
Lifestar Pharma LLC3tabletGeneric drugs (ANDA)November 1, 2023
Mylan Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)September 11, 2003
NCS HealthCare of Ky, LLC DBA Vangard Labs3tabletGeneric drugs (ANDA)August 10, 2020
Novugen Pharma (USA) LLC3tabletGeneric drugs (ANDA)October 18, 2023
PD-Rx Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)August 19, 2019
Par Health USA, LLC3tabletGeneric drugs (ANDA)October 29, 2018
Proficient Rx LP3tabletGeneric drugs (ANDA)October 15, 2020
Rising Pharma Holdings, Inc.3tabletGeneric drugs (ANDA)April 1, 2019
TruPharma, LLC3tabletGeneric drugs (ANDA)August 19, 2019
Umasuto, LLC3tabletGeneric drugs (ANDA)March 5, 2025
Upsher-Smith Laboratories, LLC3tabletGeneric drugs (ANDA)November 3, 2004
Xiromed, LLC3tabletGeneric drugs (ANDA)October 15, 2020
Zydus Lifesciences Limited3tabletGeneric drugs (ANDA)September 17, 2020
Zydus Pharmaceuticals USA Inc.3tabletGeneric drugs (ANDA)September 17, 2020
Coupler LLC1tabletGeneric drugs (ANDA)February 1, 2025
Mylan Institutional Inc.1tabletGeneric drugs (ANDA)September 11, 2006
Safecor Health, LLC1tabletGeneric drugs (ANDA)March 13, 2026

Dosage forms

Dosage formProductsShare
Tablet109100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)109100%

Pharmacologic classes

ClassProducts
alpha-Adrenergic Agonist109

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.