EUTHYROX

This brand name is authorized in Austria, Brazil, Cyprus, Germany, Estonia, Croatia, Israel, Malta, Nigeria, Netherlands, Poland, Romania, Singapore, Turkey, United States, South Africa

Active ingredients

The drug EUTHYROX contains one active pharmaceutical ingredient (API):

1 Levothyroxine UNII 9J765S329G - LEVOTHYROXINE SODIUM

Levothyroxine sodium is used for the treatment of hypothyroidism. The chief action of levothyroxine is to increase the rate of cell metabolism. Read about Levothyroxine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
EUTHYROX Tablet	Marketing Authorisation Holder	MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code	Group title	Classification
H03AA01	Levothyroxine sodium	H Systemic hormonal preparations, excl. Sex hormones and insulins → H03 Thyroid therapy → H03A Thyroid preparations → H03AA Thyroid hormones
Discover more medicines within H03AA01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 525404125112419, 525404126119417, 525404127115415, 525404128111413, 525404129118411, 525404130116419, 525404131112417, 525404132119415, 525404133115413, 525404134111411, 525404135118312, 525418120050503, 525418120050603, 525418120050703, 525418120050803, 525418120050903, 525418120051003, 525418120051103, 525418120051203, 525418120051303, 525418120051403, 525418120051503
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 01916681, 01916706, 01916729, 02050605, 02050640, 02050692, 02198012, 02292194, 02292202, 02361819, 02754677, 02754708, 02754737, 02754766, 02754795, 02754826, 02754855, 02754861, 02754878, 02754884, 03542291, 03542322, 09714250, 17267210
Country: EE	Ravimiamet	Identifier(s): 1102600, 1706352, 1827121
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-012640690, HR-H-049751832, HR-H-261403751, HR-H-303506536, HR-H-531410473, HR-H-628995193, HR-H-853297728, HR-H-867485518
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 8195, 8196, 9422
Country: MT	Medicines Authority	Identifier(s): AA565/80601, AA565/80602
Country: NG	Registered Drug Product Database	Identifier(s): A4-0147, A4-0160, A4-0161
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 15784, 15792, 23469, 24783, 34894, 48941, 60992, 61018, 90670, 90689, 90697
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100122250, 100122266, 100122303, 100122310, 100122326, 100122332, 100122349, 100122361, 100213454, 100213477, 100213483, 100262725
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W66290002, W66291003, W66292003, W66293002, W66294002, W67515001, W67515002, W67516001, W67516002
Country: SG	Health Sciences Authority	Identifier(s): 09739P, 09740P, 09741P, 11536P
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699808010032, 8699808010049, 8699808010056, 8699808010063, 8699808010070, 8699808010087, 8699808010094, 8699808010100
Country: US	FDA, National Drug Code	Identifier(s): 72305-025, 72305-050, 72305-075, 72305-088, 72305-100, 72305-112, 72305-125, 72305-137, 72305-150, 72305-175, 72305-200
Country: ZA	Health Products Regulatory Authority	Identifier(s): 52/21.3/0440, A39/21.3/0401, A39/21.3/0402, A39/21.3/0403