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Drug company (FDA labeler)

Teva Pharmaceuticals, Inc.

NDC labeler code: 0480

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

141Products (NDC)

Prescription medicines

Show the other 16 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
July 13, 2026ANDA209938 Eltrombopag
ELTROMBOPAG OLAMINE
Teva Pharms USA
June 17, 2026ANDA208815 Eltrombopag
ELTROMBOPAG OLAMINE
Actavis Labs Fl
June 8, 2026ANDA211187 Macitentan
MACITENTAN
Teva Pharms USA Inc
April 23, 2026ANDA212212 Budesonide and formoterol fumarate dihydrate
BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE
Teva Pharms USA Inc
April 15, 2026ANDA218738 Glycerol phenylbutyrate
GLYCEROL PHENYLBUTYRATE
Teva Pharms Inc
April 6, 2026ANDA211541 Dapagliflozin
DAPAGLIFLOZIN
Teva Pharms USA
March 11, 2026ANDA212563 Ferric citrate
FERRIC CITRATE
Teva Pharms USA
December 29, 2025ANDA202327 Sitagliptin
SITAGLIPTIN PHOSPHATE
Watson Labs Inc
November 13, 2025ANDA220276 Atorvastatin
ATORVASTATIN CALCIUM
Teva Pharms Inc
October 23, 2025ANDA219465 Dalbavancin
DALBAVANCIN HYDROCHLORIDE
Teva Pharms Inc
August 27, 2025ANDA211094 Dasatinib
DASATINIB
Teva Pharms USA
August 27, 2025ANDA214568 Liraglutide
LIRAGLUTIDE
Teva Pharms
May 23, 2025ANDA209801 Perampanel
PERAMPANEL
Teva Pharms USA Inc
April 8, 2025ANDA208436 Azelastine hydrochloride and fluticasone propionate
AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE
Teva Pharms USA Inc
August 22, 2024ANDA213191 Mesalamine
MESALAMINE
Teva Pharms Inc
August 16, 2024ANDA217968 Lapatinib
LAPATINIB DITOSYLATE
Teva Pharms USA Inc
July 22, 2024ANDA216456 Tiopronin
TIOPRONIN
Teva Pharms Inc
June 25, 2024ANDA204982 Phentermine and topiramate
PHENTERMINE HYDROCHLORIDE AND TOPIRAMATE
Actavis Labs Fl Inc
January 16, 2024ANDA208443 Fidaxomicin
FIDAXOMICIN
Actavis Labs Fl
December 14, 2023ANDA203880 Cyclosporine
CYCLOSPORINE
Teva Pharms USA Inc
November 29, 2023NDA216774 Eltrombopag (eltrombopag choline)
ALVAIZ
Teva Pharms Inc
October 19, 2023ANDA217517 Pazopanib
PAZOPANIB HYDROCHLORIDE
Teva Pharms Inc
August 25, 2023ANDA202802 Lisdexamfetamine dimesylate
LISDEXAMFETAMINE DIMESYLATE
Actavis Elizabeth
August 25, 2023ANDA215415 Lisdexamfetamine dimesylate
LISDEXAMFETAMINE DIMESYLATE
Teva Pharms
June 22, 2023ANDA209253 Amphetamine
AMPHETAMINE
Actavis Labs Fl Inc
Show the other 34 applications
ApprovedApplicationMedicineSponsor
May 11, 2023NDA216338 Paclitaxel
PACLITAXEL
Teva Pharms Inc
April 26, 2023ANDA208913 Gefitinib
GEFITINIB
Actavis Labs Fl Inc
March 10, 2023ANDA206210 Topiramate
TOPIRAMATE
Actavis Labs Fl
December 12, 2022ANDA211601 Tasimelteon
TASIMELTEON
Teva Pharms USA Inc
October 12, 2022ANDA216932 Tadalafil
ALYQ
Teva Pharms Inc
October 12, 2022ANDA216961 Theophylline
THEOPHYLLINE
Teva Pharms Inc
September 23, 2022ANDA207124 Deferasirox
DEFERASIROX
Teva Pharms USA
June 22, 2022ANDA209641 Adapalene and benzoyl peroxide
ADAPALENE AND BENZOYL PEROXIDE
Actavis Labs Ut Inc
May 10, 2022ANDA207588 Levothyroxine
LEVOTHYROXINE SODIUM
Watson Labs Teva
May 4, 2022ANDA209956 Pomalidomide
POMALIDOMIDE
Teva Pharms USA
January 31, 2022ANDA210876 Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE
Teva Pharms USA
January 25, 2022ANDA212759 Pirfenidone
PIRFENIDONE
Teva Pharms USA
January 18, 2022ANDA209920 Lubiprostone
LUBIPROSTONE
Teva Pharms USA Inc
August 13, 2021ANDA215506 Pyrimethamine
PYRIMETHAMINE
Teva Pharms
May 21, 2021ANDA201452 Lenalidomide
LENALIDOMIDE
Arrow Intl
November 12, 2020ANDA209567 Sorafenib
SORAFENIB TOSYLATE
Teva Pharms USA Inc
September 11, 2020ANDA209525 Icosapent ethyl
ICOSAPENT ETHYL
Teva Pharms USA
August 21, 2020NDA208419 Pemetrexed
PEMETREXED
Actavis
July 2, 2020ANDA208008 Fingolimod
FINGOLIMOD HYDROCHLORIDE
Teva Pharms USA
September 30, 2019ANDA208212 Vilazodone hydrochloride
VILAZODONE HYDROCHLORIDE
Teva Pharms USA
March 29, 2019ANDA205885 Tadalafil
TADALAFIL
Watson Labs Inc
September 4, 2018ANDA208390 Ticagrelor
TICAGRELOR
Watson Labs Inc
September 4, 2018ANDA209700 Teriflunomide
TERIFLUNOMIDE
Teva Pharms USA
October 10, 2017ANDA202934 Dextromethorphan hydrobromide and quinidine sulfate
DEXTROMETHORPHAN HYDROBROMIDE AND QUINIDINE SULFATE
Actavis Elizabeth
February 3, 2017ANDA205932 Pitavastatin
PITAVASTATIN CALCIUM
Orient Pharma Co Ltd
February 23, 2016ANDA204648 Diclofenac
DICLOFENAC POTASSIUM
Bionpharma
June 6, 2011ANDA079218 Levonorgestrel and ethinyl estradiol
LEVONORGESTREL AND ETHINYL ESTRADIOL
Watson Labs
January 15, 2008ANDA077793 Pravastatin sodium
PRAVASTATIN SODIUM
Aurobindo Pharma USA
June 28, 2007ANDA076846 Amlodipine
AMLODIPINE BESYLATE
Teva
September 12, 2003ANDA075350 Gabapentin
GABAPENTIN
Actavis Elizabeth
August 27, 2002ANDA075416 Naproxen
NAPROXEN SODIUM
Actavis Labs Fl Inc
January 12, 1973ANDA083177 Hydrochlorothiazide
HYDROCHLOROTHIAZIDE
Ivax Sub Teva Pharms
January 9, 1973ANDA080172 Propylthiouracil
PROPYLTHIOURACIL
Actavis Elizabeth
January 2, 1973NDA017060 Norethindrone
NOR-QD
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

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