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Candesartan Cilexetil/Hydrochlorothiazide

Tier C — Watch / trade

Candesartan Cilexetil/Hydrochlorothiazide

Takeda Pharmaceutical Company Limited
Originator
2000
First approval
-
Expiry (public)
No sales data
Peak sales
Small molecule
Type

Targets:Thiazide-sensitive sodium-chloride cotransporter, AT1

Brand:Ratacand plus, Atacand HCT, Atacand plus, Blopress Plus, Ecard

Indications (approved):Hypertension

Regional status

US
Approved
2000-09-05
EU
-
China
Approved
2011-01-28
Japan
Approved
2009-01-21

Factories producing this API10

Factories registered as producing this API in our sourcing network (RFQ records + product master), sorted by RFQ activity; the snapshot carries no cost or customer data.

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Synthetic routes & intermediates

Routes not yet onboarded — the daily pipeline enriches by priority (approved small molecules first); this page updates automatically.

Frequently asked questions

What are the approved indications of Candesartan Cilexetil/Hydrochlorothiazide?

Approved indications include: Hypertension.

When does the Candesartan Cilexetil/Hydrochlorothiazide patent expire?

No public expiry year is available for Candesartan Cilexetil/Hydrochlorothiazide yet; this page updates once verified.

How do I get a quote for Candesartan Cilexetil/Hydrochlorothiazide intermediates?

Open the CAS profile of the target intermediate from this page, or submit an RFQ directly — the CAS enters the matching flow automatically and the supply network responds with quotes.

Source: cross-verified data (structured fields only) · 2026-09-27