WHO-GMP sourced EU-GMP partners ISO 9001:2015 49+ export markets Since 2003

Candesartan (Atacand) is an angiotensin II receptor blocker for hypertension and heart failure, supplied as 4, 8, 16 and 32 mg tablets for oral use.

M Care Exports supplies candesartan cilexetil, sold as Atacand in the US and in Ireland and as Amias in the UK, to hospital pharmacies, importers and tender desks in the GCC, Africa and the UK. If you are looking for candesartan 8 mg or 16 mg tablets, send the destination, the strength, the pack and the quantity, and we quote per destination.

Atacand 8 mg candesartan cilexetil tablets carton, 28 tablets
WHO-GMP sourcing CDSCO licensed exporter EU-GMP capable partners Cold-chain validated (2–8°C & −25°C) CTD / eCTD dossier-ready ISO 9001:2015
Bulk supply and export terms

Candesartan exporter and bulk supplier from India.

"We need a partner for candesartan" is a typical enquiry from a hospital tender desk or a licensed importer. M Care Exports is a merchant-exporter: we supply originator or regulator-registered brands and Indian-made lines, and we confirm which one your destination's registration accepts before we quote. Candesartan is a plain oral tablet with no cold chain, so freight is simple. What moves the quote is the strength (4, 8, 16 or 32 mg), the pack, the quantity, whether you want the Atacand or Amias brand or another line, and the registration route in your country. The fixed combination with hydrochlorothiazide is a separate product and a separate line.

Source

WHO-GMP-certified Indian manufacturing line, named on every quote.

Minimum order

No blanket MOQ. Set by the source manufacturer's minimum batch-release quantity for the strength and pack ordered.

Pricing

On request. Indicative FOB or CIF quote, formal proforma on confirmation.

Incoterms

EXW, FOB, CIF, CIP or DAP.

Payment

Letter of credit (sight or usance) and telegraphic transfer.

Documentation

WHO-GMP certificate of the source line, product-specific CoPP, batch CoA, method of analysis, Free Sale Certificate, Certificate of Origin, CTD or eCTD dossier. On request.

Shelf-life

Minimum remaining shelf-life agreed per order and confirmed on the proforma.

Response

Availability and CoPP status within two working days; pre-alert documents before dispatch.

Request a bulk quote → Send a bulk enquiry by form How bulk supply works
At a glance

Angiotensin II receptor blocker (ARB), antihypertensive and heart failure treatment, sourced and documented for export.

Candesartan cilexetil is an angiotensin II receptor blocker (ARB). The US Atacand label (ANI Pharmaceuticals, Inc., distributor; manufactured by AstraZeneca AB; revision 07/25) lists two indications: hypertension in adults and in children 1 to under 17 years of age, and heart failure (NYHA class II to IV) in adults with left ventricular systolic dysfunction (ejection fraction 40% or less), to reduce cardiovascular death and heart failure hospitalisation. The US tablets are 4, 8, 16 and 32 mg. The UK emc SmPC we read for a candesartan cilexetil tablet (Milpharm) lists primary hypertension in adults, hypertension in children and adolescents aged 6 to under 18 years, and adult heart failure with ejection fraction 40% or less when ACE inhibitors are not tolerated or as add-on therapy. In the UK, the emc also lists the Amias brand of candesartan cilexetil tablets from Neon Healthcare Ltd. The Irish regulator (HPRA) lists Atacand 8 mg tablets as authorised, held by Cheplapharm Arzneimittel GmbH, with an authorisation date of 29 April 2002. Candesartan is not labelled for migraine.

Active ingredient

Candesartan cilexetil. Angiotensin II receptor blocker (ARB), antihypertensive and heart failure treatment.

Forms and strengths

4 mg tablet; 8 mg tablet; 16 mg tablet; 32 mg tablet.

Indications

Candesartan cilexetil (Atacand) is an oral angiotensin II receptor blocker used for hypertension and heart failure, as set out in the US and UK labelling.

Administration

Oral. Tablet (scored, uncoated).

Documentation

Batch-specific CoA, CoPP, manufacturing-site WHO-GMP certificate and stability data compiled per consignment, in the format the destination regulator expects.

Who we supply

Hospital pharmacies, licensed importers and tender desks across our export markets.

India is our origin. We do not sell into the Indian market.

Buyers are hospital pharmacists, MoH and hospital tender desks, and licensed importers and distributors in the GCC, Africa and the UK. Typical enquiries read "I'm looking for candesartan 16 mg tablets for a hospital tender" or "We need a partner for Atacand 8 mg". Each destination has its own registration or import route, for example the Emirates Drug Establishment (EDE) in the UAE, NAFDAC in Nigeria and the MHRA in the UK, and we align the offer with it before quoting. M Care supplies both originator or regulator-registered brands and Indian-made lines. As an example of the Indian-made lines in our catalogue, Actinsar 8 mg tablet is one; we do not claim it is registered in any destination, and registration depends on the destination regulator.

GCC registration routes

Supply against MoH registration held by your local licensed importer, or via the GCC central registration pathway.

MoH registration, GCC →

UK unlicensed routes

Where no UK licence exists, the MHRA Specials and named-patient import routes cover clinically justified demand.

MHRA Specials →

Tender desks

Bid-pack documentation assembled to the tender's specification, from CoPP to batch records.

Tender response →

Dossier support

CTD documentation from the sourcing manufacturer, compiled for your regulator's format.

Dossier preparation →

Pharmacist's note

What the dispensing pharmacist checks on candesartan.

Dose by indication, not by a single number. The US label starts adult hypertension at 16 mg once daily for patients who are not volume depleted, given once or twice daily with total daily doses of 8 to 32 mg, while the UK SmPC we read starts at 8 mg once daily, allows 4 mg in patients at risk of hypotension or with renal impairment, and recommends 4 mg in mild to moderate hepatic impairment. In heart failure both start at 4 mg once daily and double at intervals of about two weeks (UK: at least two weeks) toward 32 mg once daily, as tolerated. Paediatric hypertension has its own age bands and weight-based limits, and the US and UK age ranges differ (1 to under 17 years in the US, 6 to under 18 in the UK SmPC), so check the label of the destination. The US label carries a boxed warning on fetal toxicity: when pregnancy is detected, discontinue Atacand as soon as possible. The UK SmPC contraindicates ARBs in the second and third trimesters and does not recommend them in the first. The UK SmPC states the tablet can be divided into equal doses.

Regulatory & quality

The documentation pack a regulator actually asks for.

Candesartan is a room-temperature product. The US Atacand label gives 20 to 25 °C with excursions to 15 to 30 °C and asks for the container to be kept tightly closed. The UK emc SmPC for a candesartan cilexetil 16 mg tablet gives storage below 30 °C and a 2-year shelf life. The US label states that Atacand is a registered trademark of the AstraZeneca group of companies, licensed to ANI Pharmaceuticals, Inc., and that the tablets are manufactured by AstraZeneca AB under licence from Takeda Pharmaceutical Company, Ltd. M Care documentation covers batch certificates of analysis, export documents and destination-aligned dossier support where the regulator requires it. We state the source and quality status of each line before quoting, and make no claim for M Care itself beyond merchant-exporter documentation.

CoA and MoA, per batch

Batch-specific certificate and method of analysis from the sourcing manufacturer's QC release.

CoPP, WHO-GMP, MFG licence

Certificate of pharmaceutical product and site GMP certification issued via CDSCO channels, naming the actual manufacturing site.

CTD Module 3

Chemistry, manufacturing and controls documentation available from the sourcing manufacturer for registration filings.

Pack insert, labels, artwork

Destination-language patient information and labelling to the local regulator's standard, locked before shipment.

Pharmacovigilance

A named PV contact arranged in the destination market where the registration requires one.

How the enquiry works

Molecule · strength · volume · destination. One working day to a quote.

  1. Send us the specifics. Form and strength, pack preference, destination market and indicative volume for candesartan.
  2. We route to the right line. The enquiry goes to the WHO-GMP certified manufacturing partner whose certificates fit your regulator.
  3. Commercial and regulatory offer. FOB or CIF price with the documentation list, named manufacturing site and current certificate validity.
  4. Order, produce, release, ship. QC release on the Indian side, batch documents compiled, despatch on the agreed incoterm.
  5. After delivery. Batch records and certificates archived and retrievable for the life of the product on your shelf.
Frequently asked

Candesartan supply, the specific questions.

What decides the landed price of candesartan 8 mg for an importer?

We do not publish prices. The landed cost depends on whether you want an originator brand such as Atacand or another candesartan line, the strength (4, 8, 16 or 32 mg), the pack, the quantity, the registration route in your destination and Incoterms. Candesartan tablets need no cold chain on the US and UK labels we read, so freight is simpler than for refrigerated products. M Care Exports quotes per destination once you send the strength, volume and country.

Is there a generic candesartan, and what is the brand name?

Yes. The brand name is Atacand in the US and Ireland, and Amias in the UK. In the US, Drugs@FDA lists Atacand under NDA020838 (ANI Pharmaceuticals) and several approved generic candesartan cilexetil tablets, including from Mylan, Zydus, Alembic, Macleods and Prinston. In the UK, the emc lists Amias (Neon Healthcare Ltd) alongside candesartan cilexetil tablets sold under the ingredient name by holders such as Milpharm, Krka and Sandoz. In Ireland, the HPRA lists Atacand 8 mg tablets as authorised, held by Cheplapharm Arzneimittel GmbH. M Care Exports confirms which line is available for your destination.

What is the usual candesartan dose, and what do the 4 mg, 8 mg, 16 mg and 32 mg tablets cover?

The strengths are 4, 8, 16 and 32 mg tablets. The US Atacand label starts adult hypertension at 16 mg once daily in patients who are not volume depleted, given once or twice daily with total daily doses of 8 to 32 mg, and starts heart failure at 4 mg once daily with a target of 32 mg once daily. The UK SmPC we read starts hypertension at 8 mg once daily, up to 32 mg. Your prescriber and the destination label set the dose; we supply the strength you order.

Is candesartan used for migraine?

Migraine is not a labelled indication for candesartan. The US Atacand label lists hypertension and heart failure, and the UK SmPC we read lists primary hypertension, paediatric hypertension and heart failure. M Care Exports does not promote any use outside the labelled indications.

Is candesartan with hydrochlorothiazide the same product?

No, the combination is a separate product. In the US, Atacand HCT (candesartan cilexetil and hydrochlorothiazide) is listed on DailyMed and Drugs@FDA under NDA021093, in 16/12.5, 32/12.5 and 32/25 mg strengths, and generic combinations are approved. The US label for Atacand HCT states it is not indicated for initial therapy. If you are looking for a combination tablet, send the exact name and strengths and we confirm what your destination accepts.

Can M Care Exports supply Atacand and Indian-made candesartan, and what about pregnancy and registration?

We supply both originator or regulator-registered brands such as Atacand and Indian-made lines, for example Actinsar 8 mg tablet, where your destination's registration accepts them. We do not claim any Indian-made line is registered in a given country. The US label has a boxed warning on fetal toxicity, and the UK SmPC contraindicates use in the second and third trimesters. Registration depends on the regulator, and we confirm it per enquiry.

Sources and review

Who stands behind this page, and where its statements come from.

Reviewed by Dr. Rajat Bhatt, PharmD, Managing Director, M Care Exports. Last reviewed 2026-11-08.

This page is sourcing information for licensed importers, hospital procurement and tender desks. It is not medical, pharmaceutical or prescribing advice, and it is not a substitute for the approved product information of the line on your order. See our full disclaimer.

Candesartan enquiry

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Form and strength, destination market and indicative volume. The Mumbai desk replies within one working day, including when the honest answer is that the route is not viable yet.

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