ENAP

This brand name is authorized in Albania, Estonia, Hong Kong, Croatia, Ireland, Lithuania, Poland, Romania, Singapore, South Africa

Active ingredients

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

1 Enalapril
UNII 9O25354EPJ - ENALAPRIL MALEATE

Enalapril is hydrolysed via hepatic CES 1 to the active metabolite enalaprilat, which acts as an ACE inhibitor. ACE is a peptidyl dipeptidase which catalyses the conversion of angiotensin I to the vasoconstrictor substance angiotensin II and hence inhibition of ACE results in decreased plasma angiotensin II. This also leads to increased plasma renin activity and decreased aldosterone secretion. The mechanism of action of enalapril is therefore primarily via the suppression of the RAAS. However, ACE is identical to kininase II, and so enalapril may also exert its effects by blocking the degradation of bradykinin, a potent vasodepressor peptide.

Read about Enalapril

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ENAP Tablet Health Products Regulatory Authority (IE) 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
C09AA02 Enalapril C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09A ACE inhibitors, plain → C09AA ACE inhibitors, plain
Discover more medicines within C09AA02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AL Fondi i Sigurimit të Detyrueshëm të Kujdesit Shëndetësor Identifier(s): 87/73
Country: EE Ravimiamet Identifier(s): 1005174, 1005219, 1016929, 1016930, 1133884, 1133895, 1133907, 1133918, 1133929, 1133930, 1133941, 1133952, 1133963
Country: HK Department of Health Drug Office Identifier(s): 46138, 46139, 46140
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-026284533, HR-H-335461582, HR-H-378572738
Country: IE Health Products Regulatory Authority Identifier(s): 24041, 24052, 24073
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1003306, 1003307, 1003308, 1014198, 1019888, 1019889, 1022325, 1088355, 1092958
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100021944, 100021950, 100021967
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W02922001, W02922002, W02922003, W02923001, W02923002, W02923003, W02925001, W02925002, W02925003, W07946001, W58233001
Country: SG Health Sciences Authority Identifier(s): 11370P, 11371P
Country: ZA Health Products Regulatory Authority Identifier(s): 34/7.1.3/0085, 34/7.1.3/0086, 34/7.1.3/0087

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