TRITACE

This brand name is authorized in Austria, Australia, Hong Kong, Ireland, Israel, Mexico, Nigeria, Poland, Romania, Singapore, United Kingdom, South Africa

Active ingredients

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

1 Ramipril
UNII L35JN3I7SJ - RAMIPRIL

Ramiprilat, the active metabolite of the prodrug ramipril, inhibits the enzyme dipeptidylcarboxypeptidase I (synonyms: angiotensin-converting enzyme; kininase II). In plasma and tissue this enzyme catalyses the conversion of angiotensin I to the active vasoconstrictor substance angiotensin II, as well as the breakdown of the active vasodilator bradykinin. Reduced angiotensin II formation and inhibition of bradykinin breakdown lead to vasodilatation.

Read about Ramipril

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
TRITACE 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
C09AA05 Ramipril C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09A ACE inhibitors, plain → C09AA ACE inhibitors, plain
Discover more medicines within C09AA05

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): 1316G, 1944H, 1945J, 1946K, 8470T
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 136013, 136014, 136015, 13802, 13806, 30401, 337642, 337648, 337650, 337652, 50106, 50109, 50112, 50115
Country: HK Department of Health Drug Office Identifier(s): 36855, 36856
Country: IE Health Products Regulatory Authority Identifier(s): 48017, 48023, 48042, 48061, 48122, 48166, 48175, 48189
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 2658, 2659, 2660
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 040M92
Country: NG Registered Drug Product Database Identifier(s): 04-2850, A4-4105
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100093257, 100093263, 100105871, 100403210, 100419078, 100419552, 100423826, 100424889, 100433664, 100447100, 100450128, 100454405, 100456819, 100467064, 100467096, 100468189, 100468437
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W62382001, W62382002, W62382003, W62382004, W62382005, W62382006, W62382007, W62382008, W62382009, W62382010, W62382011, W62382012, W62382013, W62382014, W62382015, W62382016, W62382017, W62382018, W62382019, W62447001, W62447002, W62447003, W62447004, W62447005, W62447006, W62447007, W62447008, W62447009, W62447010, W62447011, W62447012, W62447013, W62447014, W62447015, W62447016, W62447017, W62447018, W62447019, W62447020, W62447021, W62451001, W62451002, W62451003, W62451004, W62451005, W62451006, W62451007, W62451008, W62451009, W62451010, W62451011, W62451012, W62451013, W62451014, W62451015, W62451016, W62451017, W62451018, W62451019
Country: SG Health Sciences Authority Identifier(s): 09591P, 09592P
Country: ZA Health Products Regulatory Authority Identifier(s): 31/7.1.3/0667, W/7.1.3/235

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