Regulatory PathRegulatory requirements compared

Active substance

Tranylcypromine

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
PARNATE 10 MG. TAB.10 mgTablet · Oral use50 BlisterSAR 16.85NCE · PrescriptionSMIITHKLINE BEECHAMWithdrawn by MAH · Not Marketed

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
PARNATEEQ 10MG BASEtablet · oralADVANZ PHARMAPrescription21 Feb 1961
TRANYLCYPROMINE SULFATEEQ 10MG BASEtablet · oralSTRIDES PHARMA INTLPrescription29 Jun 2006
TRANYLCYPROMINE SULFATEEQ 10MG BASEtablet · oralNOVITIUM PHARMAPrescription17 Apr 2018
TRANYLCYPROMINE SULFATEEQ 10MG BASEtablet · oralCROSSMEDIKA SAPrescription27 Jun 2022

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
M-TRANYLCYPROMINE0254218810 MGTABLET · ORALMANTRA PHARMA INC
PARNATE0191959810 MGTABLET · ORALGLAXOSMITHKLINE INC

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACTRANYLCYPROMINE SULF 10 MG TAB$0.5911per EA23 Sep 2026
NHS Drug TariffTranylcypromine 10mg tablets£485.0028 tablet1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

Safety signals and safety-related labeling changes

  • US FDA 4 Jan 2018 PARNATE — safety-related labeling change
    Labeling sections changed: Boxed Warning; Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide

All safety entries for tranylcypromine →

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.