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Drug company (FDA labeler)

Perfero Pharma, Inc.

NDC labeler code: 87143

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

4Products (NDC)

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
September 13, 2022ANDA214136 Tazarotene
TAZAROTENE
Cosette Pharms Nc
May 11, 2020ANDA210765 Calcipotriene and betamethasone dipropionate (betamethasone dipropionate / calcipotriene)
CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE
Cosette Pharms Nc
November 21, 2017ANDA209556 Hydrocortisone butyrate
HYDROCORTISONE BUTYRATE
The J Molner
March 24, 2011ANDA078468 Calcipotriene
CALCIPOTRIENE
Cosette Pharms Nc

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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