Skip to the page

Data / Drug companies / Phendimetrazine tartrate

Phendimetrazine tartrate: 13 companies and 20 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Phendimetrazine tartrate is listed in the FDA National Drug Code Directory by 13 companies, with 20 products in commercial distribution. 19 of the products (95.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; capsule, extended release, and the newest product started marketing on November 1, 2022.

The request: Get every company that lists phendimetrazine tartrate in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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
13
Products
20
Generic (ANDA) products
19 (95.0%)
Application numbers
4
Controlled substance schedule
Schedule III
Routes
Oral
openFDA record search
api.fda.gov

Companies that list phendimetrazine tartrate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions3tabletGeneric drugs (ANDA)September 15, 2010
Bryant Ranch Prepack3tabletGeneric drugs (ANDA)July 1, 2018
KVK-Tech, Inc.3tabletGeneric drugs (ANDA)September 15, 2010
NuCare Pharmaceuticals,Inc.2tabletGeneric drugs (ANDA)November 20, 2012
Acertis Pharmaceuticals, LLC1capsule, extended releaseNew drug applications (NDA)November 1, 2022
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)November 20, 2012
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)July 1, 2018
Calvin Scott & Co., Inc.1tabletGeneric drugs (ANDA)January 1, 1978
Elite Laboratories, Inc.1tabletGeneric drugs (ANDA)November 20, 2012
NuCare Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)September 15, 2010
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)September 15, 2010
Preferred Pharmaceuticals Inc.1tabletGeneric drugs (ANDA)August 13, 2018
Virtus Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)July 1, 2018

Dosage forms

Dosage formProductsShare
Tablet1995%
Capsule, extended release15%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1995%
New drug applications (NDA)15%

Pharmacologic classes

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.