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MedsAcross

Medicine

Atacand 4 mg tablet

Candesartan cilexetil · Oral · ANI Pharmaceuticals
Available on requestPrescription onlyUS FDA

Atacand 4 mg tablet is a prescription medicine containing Candesartan cilexetil for oral use, marketed by ANI Pharmaceuticals, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store at 20° to 25°C (68° to 77°F), excursions permitted at 15° to 30°C (59°…

Key facts

Active ingredient (INN)
Candesartan cilexetil
Brand
Atacand
Strength
4 mg
Dosage form
Tablet
Route
Oral
Packs
30 tablets
Marketing authorisation holder
ANI Pharmaceuticals
Manufacturer
ANI Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20° to 25°C (68° to 77°F), excursions permitted at 15° to 30°C (59° to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 October 2018
Identifiers
RxCUI 153822, 153823, 577776 +5DailyMed set ID 94a59260-d2b6-464a-b5b9-bbc599e57e10NDC 62559-640Application NDA020838

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

PackCodeLabelerMarketed since
30 tablet in 1 bottle62559-640-30ANI Pharmaceuticals1 October 2018

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 4 June 1998Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Candesartan cilexetil 4 mg tablet.

Compare 1

Other strengths and forms of Candesartan cilexetil

Clinical summary

Candesartan cilexetil is an angiotensin 2 receptor blocker indicated for treatment of hypertension in adults and children 1 to < 17 years of age, to lower blood pressure, among other approved uses. MedsAcross supplies Candesartan cilexetil for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Candesartan cilexetil

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

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