Regulatory PathRegulatory requirements compared

Active substance

Amcinonide

Open in the medicines table

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

ProductStrengthForm · routeApplicantStatusFirst approved
AMCINONIDE0.1%cream · topicalTARO PHARM INDSPrescription31 May 2002
AMCINONIDE0.1%lotion · topicalSOLUBIOMIXPrescription6 Nov 2002
AMCINONIDE0.1%ointment · topicalGENUSPrescription19 Nov 2002
CYCLOCORT0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**cream · topicalASTELLASDiscontinued18 Oct 1979
CYCLOCORT0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**ointment · topicalASTELLASDiscontinued13 Nov 1981
CYCLOCORT0.1%lotion · topicalASTELLASDiscontinued13 Jun 1988
AMCINONIDE0.1%ointment · topicalTARO PHARM INDSDiscontinued19 Mar 2003
AMCINONIDE0.1%cream · topicalGENUS LIFESCIENCESDiscontinued15 May 2003

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
TARO-AMCINONIDE022467140.1 %CREAM · TOPICALTARO PHARMACEUTICALS INC

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACAMCINONIDE 0.1% CREAM$4.90193per GM17 Jun 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.

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.