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Drug company (FDA labeler)

Zameer Pharmaceuticals LLC

NDC labeler code: 90096

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

16Products (NDC)

Prescription medicines

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
April 29, 2026ANDA218341 Oxcarbazepine
OXCARBAZEPINE
Umedica Labs Pvt
July 25, 2023ANDA213085 Ranolazine
RANOLAZINE
Piramal
February 16, 2022ANDA215781 Trospium chloride
TROSPIUM CHLORIDE
Chartwell Rx
November 29, 2021ANDA212630 Chlorpromazine hydrochloride
CHLORPROMAZINE HYDROCHLORIDE
Chartwell Rx
October 20, 2021ANDA215141 Fluphenazine hydrochloride
FLUPHENAZINE HYDROCHLORIDE
Chartwell Rx
October 14, 1994NDA020067 Naproxen
EC-NAPROSYN
Atnahs Pharma Us

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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