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Profile for Tradename: ATACAND

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Atacand is a drug marketed by Astrazeneca and is included in two NDAs. It is available from eight suppliers. There is one patent protecting this drug and three Paragraph IV challenges.

The generic ingredient in ATACAND is candesartan cilexetil; hydrochlorothiazide. There are twenty-one drug master file entries for this compound. Four suppliers are listed for this compound. There is one tentative approval for this compound. Additional details are available on the candesartan cilexetil; hydrochlorothiazide profile page.

Summary for Tradename: ATACAND

Suppliers / Packagers: see list28

Pharmacology for Tradename: ATACAND

Clinical Trials for: ATACAND

CKD-330 Drug-Drug Interaction Study (Candesartan)
Status: Completed Condition: Hypertension

Atacand Dose Ranging in Hypertensive Pediatric Subjects 1 Year to Less Than 6 Years of Age
Status: Completed Condition: Hypertension

Relative Bioavailability Study of Candesartan Cilexetil Under Fasting Conditions
Status: Completed Condition: Respiratory Disorders

ARIA (Atacand Renoprotection In NephropAthy Pt.)
Status: Completed Condition: Non-diabetic Nephropathy With Hypertension

Evaluation of the Pharmacokinetic Interaction Between Candesartan and Felodipine After Ingestion of a Specific Meal
Status: Completed Condition: Healthy

Antihypertensive Efficacy and Safety of Candesartan/HCT 32/25 mg in Comparison With Individual Components and Placebo
Status: Completed Condition: Hypertension

Pivotal Bioequivalence FDC Nifedipine / Candesartan vs. Loose Combination of Single Components, Fed
Status: Completed Condition: Hypertension

Candesartan Effect in Second Stage Arterial Hypertension
Status: Completed Condition: Stage II Hypertension

Pharmacokinetic Interactions of Candesartan Cilexetil and Amlodipine Besylate
Status: Active, not recruiting Condition: Healthy

Atacand (Candesartan) Real Life Study
Status: Completed Condition: Hypertension

Courtesy of
See more clinical trials for this drug
Applicant Tradename Generic Name Dosage NDA Approval Date Type RLD Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
candesartan cilexetil
TABLET;ORAL020838-001Jun 4, 1998RXNo<disabled><disabled>
candesartan cilexetil; hydrochlorothiazide
TABLET;ORAL021093-003May 16, 2008RXYes5,721,263<disabled>Y <disabled>
candesartan cilexetil
TABLET;ORAL020838-004Jun 4, 1998RXYes<disabled><disabled>
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Paragraph IV activity for: ATACAND

Drugname Dosage Strength RLD Submissiondate
candesartan cilexetil and hydrochlorothiazideTablets32 mg/25 mgAtacand HCT3/6/2009
candesartan cilexetil and hydrochlorothiazideTablets16 mg/12.5 mg and 32 mg/12.5 mgAtacand HCT6/25/2008
candesartan cilexetilTablets4 mg, 8 mg, 16 mg and 32 mgAtacand12/22/2006
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Preferred citation:

Friedman, Y. Location of pharmaceutical innovation: 2000–2009 Nature Reviews Drug Discovery 9, 835–836 (2010).

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