Sulindac

Koutonin Tablets 200MG (Sulindac) "Central"

錠劑TaiwanCancelledAuthorised 21 Feb 1995

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In other countries

The same active substances on other registers, the same brand first.

Teva-SulindacCanada · 150 MG · Tablet · Teva Canada LimitedSame substance
Teva-SulindacCanada · 200 MG · Tablet · Teva Canada LimitedSame substance
Apo-Sulin Tab 150MGCanada · 150 MG · Tablet · Apotex INCSame substance
Clinoril Tab 200MGSaudi Arabia · Merck Sharp & DohmeSame substance
SulindacUnited States · 150MG, 200MG · tablet · Ani PharmsSame substance
ClinorilUnited States · 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · tablet · Merck

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Sulindac

Koutonin Tablets 200MG (Sulindac) "Central"

錠劑TaiwanCancelledAuthorised 21 Feb 1995

Ask Osler about it

This page is kept for reference and is not offered to search engines.

In other countries

The same active substances on other registers, the same brand first.

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Discover Osler

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

Taiwan Food and Drug Administration

TFDA, dataset 9122, Government Open Data Licence 1.0; source update and retrieval dates

Licence: Taiwan Government Open Data Licence 1.0 · Added 7 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Sulindac
Dosage form: 錠劑
Register: Taiwan (TFDA)
Status: Cancelled
Status in the register: 已註銷
Authorised: 21 Feb 1995
Registration: 衛署藥製字第038598號
Marketing authorisation holder: 中央製藥股份有限公司
Procedure: 製　劑