MedPath

Nitrendipine

Generic Name
Nitrendipine
Drug Type
Small Molecule
Chemical Formula
C18H20N2O6
CAS Number
39562-70-4
Unique Ingredient Identifier
9B627AW319

Overview

Nitrendipine is a calcium channel blocker with marked vasodilator action. It is an effective antihypertensive agent and differs from other calcium channel blockers in that it does not reduce glomerular filtration rate and is mildly natriuretic, rather than sodium retentive.

Indication

For the treatment of mild to moderate hypertension

Associated Conditions

  • Hypertension

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2021/06/18
Phase 4
Recruiting
Shanghai Jiao Tong University School of Medicine
2014/08/15
Phase 4
UNKNOWN
2009/05/05
Phase 4
Withdrawn
University of Erlangen-Nürnberg Medical School
2008/09/12
Phase 3
Completed
Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
NITRENDIPINO STADA 20 mg COMPRIMIDOS EFG
Laboratorio Stada S.L.
58172
COMPRIMIDO
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
ENIT 10 mg/20 mg COMPRIMIDOS
64506
COMPRIMIDO
Medicamento Sujeto A Prescripción Médica
Commercialized
ENEAS 10 mg/20 mg COMPRIMIDOS
64505
COMPRIMIDO
Medicamento Sujeto A Prescripción Médica
Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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