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Drug company (FDA labeler)

Allegis Holdings LLC

NDC labeler code: 71297

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

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
October 16, 2023ANDA216569 Clotrimazole
CLOTRIMAZOLE
Sciegen Pharms
February 27, 2001ANDA040396 Hydrocortisone acetate cream
MICORT-HC
Legacy
August 6, 1984NDA050575 Amoxicillin and clavulanate potassium (amoxicillin / clavulanate)
AUGMENTIN '125', AUGMENTIN '250'
Us Antibiotics
February 28, 1973ANDA083231 Hydrocortisone
ALA-SCALP
Legacy

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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