SYNTHROID

This brand name is authorized in United States. It is also authorized in Brazil, Canada, Ecuador, Israel, Mexico, New Zealand, South Africa.

Active ingredients

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

1
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 more about Levothyroxine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 SYNTHROID Tablet MPI, US: SPL/PLR FDA, National Drug Code (US)

Medicine classification

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

ATC Group 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)
BR Câmara de Regulação do Mercado de Medicamentos 500207401111413, 500207403114411, 500207404110418, 500207406113414, 500207408116410, 500207409112419, 500207410110416, 500207412113412, 500207414116419, 500207416119415, 500207417115316, 500221070046403, 500221070046503, 500221070046603, 500221070046703, 500221070046803
CA Health Products and Food Branch 02171228, 02172062, 02172070, 02172089, 02172097, 02172100, 02172119, 02172127, 02172135, 02172143, 02172151, 02233852
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 6015-MEE-0321, 6093-MEE-0321, 6101-MEE-0421, 6102-MEE-0421, 6174-MEE-0421, 6175-MEE-0421, 6176-MEE-0421, 6178-MEE-0421, 6179-MEE-0421, 6180-MEE-0421, 6279-MEE-0521
IL מִשְׂרַד הַבְּרִיאוּת 8641, 8642
MX Comisión Federal para la Protección contra Riesgos Sanitarios 127M2015
NZ Medicines and Medical Devices Safety Authority 13688, 13689, 13690, 13691, 13692, 13693, 13694, 13695, 13696, 13697, 13698, 13699
US FDA, National Drug Code 0074-3727, 0074-4341, 0074-4552, 0074-5182, 0074-6594, 0074-6624, 0074-7068, 0074-7069, 0074-7070, 0074-7148, 0074-7149, 0074-9296
ZA Health Products Regulatory Authority 42/21.3/0670, 42/21.3/0671, 42/21.3/0672, 42/21.3/0673, 42/21.3/0674, 42/21.3/0675, 42/21.3/0676, 42/21.3/0677, 42/21.3/0678, 42/21.3/0679, 42/21.3/0680, 42/21.3/0681

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