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Drug company (FDA labeler)

Orbicular Pharmaceutical Technologies Private Limited

NDC labeler code: 81607

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

6Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
August 27, 2026ANDA220938 Neomycin sulfate, polymyxin b sulfate and hydrocortisone
NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
Orbicular Pharm Tech
March 13, 2026ANDA216298 Phytonadione
PHYTONADIONE
Orbicular
February 24, 2026ANDA217234 Liraglutide
LIRAGLUTIDE
Orbicular
January 14, 2026ANDA217590 Liraglutide
LIRAGLUTIDE
Orbicular
April 20, 2023ANDA217413 Arsenic trioxide
ARSENIC TRIOXIDE
Msn

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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