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Drug company (FDA labeler)

TOLMAR Inc.

NDC labeler codes: 62935, 69087

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

8Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
May 1, 2020NDA213150 Leuprolide acetate
FENSOLVI KIT
Tolmar
March 27, 2019NDA206089 Testosterone undecanoate
JATENZO
Tolmar
December 14, 2004NDA021731 Leuprolide acetate
ELIGARD KIT
Tolmar
February 13, 2003NDA021488 Leuprolide acetate
ELIGARD KIT
Tolmar
July 24, 2002NDA021379 Leuprolide acetate
ELIGARD KIT
Tolmar
January 23, 2002NDA021343 Leuprolide acetate
ELIGARD KIT
Tolmar

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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