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Drug company (FDA labeler)

Method Pharmaceuticals, LLC

NDC labeler code: 58657

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

64Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
March 14, 2024ANDA218412 Phenylephrine
PHENYLEPHRINE HYDROCHLORIDE
Hainan Poly
March 30, 2021ANDA213827 Metolazone
METOLAZONE
Innogenix
October 9, 2020ANDA212378 Baclofen
BACLOFEN
Andas 5 Holding
March 8, 2019ANDA211064 Folic acid
FOLIC ACID
Rising
October 16, 2018ANDA209108 Cyproheptadine
CYPROHEPTADINE HYDROCHLORIDE
Pharmazone
July 20, 2018ANDA211181 Pyridostigmine bromide
PYRIDOSTIGMINE BROMIDE
Mlv
June 22, 2018ANDA208921 Ciprofloxacin
CIPROFLOXACIN HYDROCHLORIDE
Pharmobedient
March 20, 2018ANDA209781 Levetiracetam
LEVETIRACETAM
Hainan Poly Pharm
February 18, 2016ANDA204989 Gabapentin
RELGAABI
Sciegen Pharms
September 11, 2013ANDA203769 Metformin hydrochloride
METFORMIN HYDROCHLORIDE
Sciegen Pharms
June 13, 2013ANDA202297 Clonidine
CLONIDINE HYDROCHLORIDE
Yung Shin Pharm
December 22, 2009ANDA078786 Carvedilol
CARVEDILOL
Mlv
July 29, 1999ANDA075215 Labetalol
LABETALOL HYDROCHLORIDE
Innogenix
May 30, 1997ANDA074677 Captopril
CAPTOPRIL
Andas 5 Holding
January 7, 1988ANDA071173 Haloperidol
HALOPERIDOL
Sciegen Pharms
July 16, 1986ANDA070772 Metronidazole
METRONIDAZOLE
Innogenix

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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