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Drug company (FDA labeler)

Melinta Therapeutics, LLC

NDC labeler code: 70842

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

11Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
March 22, 2023NDA217417 Rezafungin
REZZAYO
Mundipharma
March 12, 2021NDA214155 Oritavancin
KIMYRSA
Melinta Therap
August 29, 2017NDA209776 Meropenem-vaborbactam
VABOMERE
Rempex
June 19, 2017NDA208610 Delafloxacin meglumine
BAXDELA
Melinta
June 19, 2017NDA208611 Delafloxacin meglumine
BAXDELA
Melinta
August 6, 2014NDA206334 Oritavancin
ORBACTIV
Melinta Therap
January 10, 1992NDA019962 Metoprolol
TOPROL-XL
Melinta Therap
October 26, 1972NDA050444 Minocycline hydrochloride
MINOCIN
Rempex

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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