OMNIC

This brand name is authorized in Brazil, Croatia, Cyprus, Estonia, Finland, Germany, Israel, Italy, Malta, Netherlands, Poland, Romania, Spain, Tunisia.

Active ingredients

The drug OMNIC 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
OMNIC Modified release capsule, hard	MPI, EU: SmPC	Web Search

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)
BR	Câmara de Regulação do Mercado de Medicamentos	540300301112415, 540300302119413, 540300303115411
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	01096864, 01419126, 02649561, 06308325, 06308348, 06551942, 06551959, 06846577, 09265473, 11647242, 12388699, 12738975
EE	Ravimiamet	1154528, 1154539
ES	Centro de información online de medicamentos de la AEMPS	61426, 66678
FI	Lääkealan turvallisuus- ja kehittämiskeskus	005108, 020238, 020338, 374348
HR	Agencija za lijekove i medicinske proizvode	HR-H-245554985, HR-H-896410977
IL	מִשְׂרַד הַבְּרִיאוּת	3727, 6004
IT	Agenzia del Farmaco	032647024, 045943014
MT	Medicines Authority	MA1387/00101, MA1387/00102, PI1438/02501A, PI908/12101B
NL	Z-Index G-Standaard, PRK	76236
PL	Rejestru Produktów Leczniczych	100075851, 100136340
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W43106001
TN	Direction de la Pharmacie et du Médicament	4453011