CIPRAMIL

This brand name is authorized in Australia, Brazil, Germany, Estonia, Ireland, Israel, Netherlands, New Zealand, Poland, United Kingdom, South Africa

Active ingredients

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

1 Citalopram
UNII I1E9D14F36 - CITALOPRAM HYDROBROMIDE

Citalopram is the most Selective Serotonin Reuptake Inhibitor (SSRI) yet described, with no, or minimal, effect on noradrenaline (NA), dopamine (DA) and gamma aminobutyric acid (GABA) uptake.

Read about Citalopram

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
CIPRAMIL Film-coated tablet Medicines & Healthcare Products Regulatory Agency (GB) 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
N06AB04 Citalopram N Nervous system → N06 Psychoanaleptics → N06A Antidepressants → N06AB Selective serotonin reuptake inhibitors
Discover more medicines within N06AB04

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 8220P
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 524200102116311
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 01229667, 01229673, 01229696, 01265700, 01265717, 02459122, 02459139, 02459145, 02558717, 03792728, 03792734, 03793113, 07528431, 07528448, 08691972
Country: EE Ravimiamet Identifier(s): 1070525
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 138495, 14215, 144960, 144962, 161491, 27300
Country: IE Health Products Regulatory Authority Identifier(s): 18304, 18310, 18351, 18359, 18382, 18395
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 3340, 6498
Country: NL Z-Index G-Standaard Identifier(s): 14271079
Country: NL Z-Index G-Standaard, PRK Identifier(s): 44083, 44091, 52485
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 7804
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100001120
Country: ZA Health Products Regulatory Authority Identifier(s): 29/1.2/0232

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