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Drug company (FDA labeler)

Patrin Pharma, Inc.

NDC labeler code: 39328

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

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
July 28, 2023ANDA203973 Calcitriol
CALCITRIOL
Anda Repository
February 18, 2022ANDA212604 Pregabalin
PREGABALIN
Anda Repository
August 20, 2021ANDA214178 Amantadine
AMANTADINE HYDROCHLORIDE
Pharmobedient
April 10, 2020ANDA210764 Methylphenidate
METHYLPHENIDATE HYDROCHLORIDE
Anda Repository
October 16, 2018ANDA209108 Cyproheptadine
CYPROHEPTADINE HYDROCHLORIDE
Pharmazone
April 11, 2018ANDA210736 Fluocinolone acetonide
FLAC
Anda Repository
January 15, 2009ANDA078582 Levetiracetam
LEVETIRACETAM
Strides Pharma

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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