NIFELAT

This brand name is authorized in Cyprus, Hong Kong, Malta, Singapore

Active ingredients

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

1 Nifedipine
UNII I9ZF7L6G2L - NIFEDIPINE

Nifedipine is a calcium antagonist of the 1,4-dihydropyridine type. Calcium antagonists reduce the transmembranal influx of calcium ions through the slow calcium channel into the cell. As a specific and potent calcium antagonist, nifedipine acts particularly on the cells of the myocardium and the smooth muscle cells of the coronary arteries and the peripheral resistance vessels. The main action of nifedipine is to relax arterial smooth muscle, both in the coronary and peripheral circulation. Nifedipine Tablets are formulated to achieve controlled delivery of nifedipine in a release profile sufficient to enable once-daily administration to be effective in clinical use.

Read about Nifedipine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
NIFELAT Film-coated tablet Υπουργείο Υγείας (CY) 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
C08CA05 Nifedipine C Cardiovascular system → C08 Calcium channel blockers → C08C Selective calcium channel blockers with mainly vascular effects → C08CA Dihydropyridine derivatives
Discover more medicines within C08CA05

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: HK Department of Health Drug Office Identifier(s): 51195
Country: MT Medicines Authority Identifier(s): MA084/01501, MA084/01503
Country: SG Health Sciences Authority Identifier(s): 07228P

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