TANYZ

This brand name is authorized in Albania, Croatia, Estonia, Ireland, Lithuania, Poland, Romania.

Active ingredients

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

1	Tamsulosin UNII 11SV1951MR - TAMSULOSIN HYDROCHLORIDE
	Tamsulosin binds selectively and competitively to post-synaptic α1-adrenoreceptors, prevailingly their subtypes designated α1A and α1D. Thus relaxation of smooth muscles of the prostate and urethra is achieved, which leads to a reduction of tonus and an improvement of the urinary flow.
	Read more about Tamsulosin

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
TANYZ Hard modified-release capsule	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group		Classification
G04CA02	Tamsulosin	G Genito urinary system and sex hormones → G04 Urologicals → G04C Drugs used in benign prostatic hypertrophy → G04CA Alpha-adrenoreceptor antagonists
Discover more medicines within G04CA02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
AL	Fondi i Sigurimit të Detyrueshëm të Kujdesit Shëndetësor	120/73
EE	Ravimiamet	1188211, 1188222, 1188233, 1188244, 1188255, 1188266, 1188277, 1188288, 1188299, 1188301, 1188312, 1435979, 1435980, 1435991, 1436004, 1436015, 1436026, 1436037, 1436048, 1436059, 1436060
HR	Agencija za lijekove i medicinske proizvode	HR-H-612679230, HR-H-951003813
IE	Health Products Regulatory Authority	37606
LT	Valstybinė vaistų kontrolės tarnyba	1004744, 1020858, 1020859, 1020860, 1020861, 1020862, 1020863, 1020864, 1020865, 1020866, 1020867, 1020868, 1020869, 1020870, 1020871, 1020872, 1020873, 1020874, 1020875, 1020876, 1020877, 1020878, 1050349, 1060265, 1060266, 1060267, 1060268, 1060269, 1060270, 1060271, 1060272, 1060273
PL	Rejestru Produktów Leczniczych	100158198, 100242496
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W42987001, W42987002, W42987003