This brand name is authorized in Nigeria.
The drug NORMODIPIN contains one active pharmaceutical ingredient (API):
1
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UNII
I9ZF7L6G2L - NIFEDIPINE
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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. |
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This drug has been approved in Nigeria as follows:
| Identifier | Form | Presentation | Description | Approval |
|---|---|---|---|---|
| A4-3639 | Prolonged-release tablet | Normodipin Tablet TAB_DR 20 mg 3x10 | 73 RNW-PP-23161 Normodipin Tablet NIFEDIPIN USP 20MG NIFEDIPINE EXTENDED RELEASE TABLET USP 20MG (Each uncoated extended release tablets contains: Nifedipine USP 20mg Excipients Q.S. A4-3639 Drugs Imported Products 310 Prescription Only Medicine (POM) 2/8/2022 MERIT HEALTHCARE LTD, Iya-Oba House, 10 Dele Ashiru Street, Ire-Akari Estate, Isolo 8171273639 casmolar1@yahoo.com Stallion Laboratories Pvt. Ltd, CIB- 305/2 & 3, G.I.D.C Kerela (Bavla). Dist; Ahmedabad Gujarat. India, India | 27/07/2023 |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| C08CA05 | Nifedipine | C Cardiovascular system → C08 Calcium channel blockers → C08C Selective calcium channel blockers with mainly vascular effects → C08CA Dihydropyridine derivatives |
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 | A4-3639 |
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