Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Drug company (FDA labeler)

Teva Respiratory, LLC

NDC labeler code: 59310

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

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
ApprovedApplicationMedicineSponsor
August 3, 2017NDA207921 Beclomethasone dipropionate HFA
QVAR REDIHALER
Norton Waterford
January 27, 2017NDA208799 Fluticasone propionate and salmeterol
AIRDUO DIGIHALER, AIRDUO RESPICLICK
Teva Pharm
March 23, 2016BLA761033 Reslizumab
CINQAIR
Teva Respiratory LLC
March 31, 2015NDA205636 Albuterol sulfate
PROAIR DIGIHALER, PROAIR RESPICLICK
Teva Branded Pharm
March 23, 2012NDA202813 Beclomethasone dipropionate HFA
QNASL
Teva Branded Pharm

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

FDA Enforcement Report search → · Report an error →