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Drug company (FDA labeler)

A2A Integrated Pharmaceuticals

NDC labeler code: 73141

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

9Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
January 17, 2024ANDA215988 Hydralazine hydrochloride and isosorbide dinitrate
ISOSORBIDE DINITRATE AND HYDRALAZINE HYDROCHLORIDE
Pharmazone
October 5, 2023ANDA216828 Guanfacine
GUANFACINE HYDROCHLORIDE
Pharmazone
August 28, 2023ANDA216488 Posaconazole
POSACONAZOLE
Pharmazone
August 17, 2023ANDA217114 Maraviroc
MARAVIROC
Pharmazone
April 27, 2022ANDA213517 Ranolazine
RANOLAZINE
Pharmazone
April 1, 1997ANDA074672 Selegiline
SELEGILINE HYDROCHLORIDE
Pharmazone

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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