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Drug company (FDA labeler)

Avet Pharmaceuticals Inc.

NDC labeler code: 23155

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

10Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
September 14, 2020ANDA212173 Acyclovir
ACYCLOVIR
Pharmobedient
March 6, 2020ANDA211412 Celecoxib
CELECOXIB
Pharmobedient
November 14, 2018ANDA205869 Letrozole
LETROZOLE
Pharmobedient
November 9, 2018ANDA206037 Anastrozole
ANASTROZOLE
Pharmobedient
November 3, 2004ANDA076725 Midodrine hydrochloride
ORVATEN
Beijing Yiling

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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