LODIVASC

This brand name is authorized in Nigeria.

Active ingredients

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

1
UNII 864V2Q084H - AMLODIPINE BESYLATE
 

Amlodipine is a calcium ion influx inhibitor of the dihydropyridine group (slow channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac and vascular smooth muscle.

 
Read more about Amlodipine

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
A4-1804 Tablet LODIVASC TABLET TAB 5 mg 110,1010 32 CMS-PP-336925 LODIVASC TABLET AMLODIPINE 5MG Amlodipine Besylate 6.94mg Pre-gelatinized Starch 25mg Vivasol GF 9.44mg Dicalcium Phosphate 65mg Magnesium Stearate 5.13mg Aerosil 200 2.50mg MCC (102) 116mg A4-1804 Drugs Nigerian Products 110,1010 POM 1 6/20/2023 MAY & BAKER NIGERIA PLC, SAPARA STREET, INDUSTRIAL ESTATE, IKEJA LAGOS LAGOS 18980079 tooluwasanmi@gmail.com May & Baker Nigeria Plc., 1 MAY & BAKER AVENUE, OTA OGUN STATE, Nigeria 28/09/2023
A4-1805 Tablet LODIVASC TABLETS TAB 10 mg 110,1010 31 CMS-PP-336921 LODIVASC TABLETS AMLODIPINE BESYLATE 10MG Amlodipine Besylate 13.87mg Pre-gelatinized Starch 25mg Vivasol GF 7.50mg Dicalcium Phosphate 60mg Magnesium Stearate 5.13mg Aerosil 200 2.50mg MCC (102) 116mg A4-1805 Drugs Nigerian Products 110,1010 POM 1 6/20/2023 MAY & BAKER NIGERIA PLC, SAPARA STREET, INDUSTRIAL ESTATE, IKEJA LAGOS LAGOS 18980079 tooluwasanmi@gmail.com May and Baker Nigeria PLC, 1 May & Baker Avenue Idiroko (opp convenant university )Ota Ogun State. P.M.B 21049, Nigeria 28/09/2023
A4-5280 Tablet Lodivasc-10 Tablets TAB 10 mg 21/12/2020

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
C08CA01 Amlodipine C Cardiovascular system → C08 Calcium channel blockers → C08C Selective calcium channel blockers with mainly vascular effects → C08CA Dihydropyridine derivatives
Discover more medicines within C08CA01

Authorization and marketing

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

Country Identification scheme Identifier(s)
NG Registered Drug Product Database A4-1804, A4-1805, A4-5280

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