Angina Pectoris
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Sign up freeTop drugs studied for this disease
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FDA approval · 2008-07-24FDA Approved: LOPRESSOR — Supplemental Application (Validus Pharmaceuticals LLC)
The FDA approved a supplemental application for Lopressor (metoprolol tartrate) from Validus Pharmaceuticals LLC.
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CLINICAL_TRIALS trial_result · 2008-05-16Clinical Trial Update: Pilot Study of Hemoglobin Based Oxygen Therapeutics in Elective Coronary Revascularization [Phase 2]
Phase 2 pilot study of hemoglobin-based oxygen therapeutics in elective coronary revascularization has completed, evaluating safety and pote…
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FDA approval · 2008-04-29FDA Approved: TENORMIN — Supplemental Application (Almatica Pharma LLC)
FDA approved a supplemental application for TENORMIN (atenolol) submitted by Almatica Pharma LLC.
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FDA approval · 2008-04-29FDA Approved: METOPROLOL TARTRATE — Original Application (Hospira, Inc.)
FDA approves Hospira's original application for metoprolol tartrate as a generic product.
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FDA approval · 2008-04-14FDA Approved: AMLODIPINE BESYLATE — Supplemental Application (Teva Pharmaceuticals, Inc.)
The FDA approved a supplemental application for amlodipine besylate from Teva Pharmaceuticals, approving a generic version of the drug. This…
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FDA approval · 2008-03-20FDA Approved: PROPRANOLOL HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals NY LLC)
FDA approves a supplemental application for propranolol hydrochloride from Amneal Pharmaceuticals NY LLC.
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FDA approval · 2008-03-20FDA Approved: PROPRANOLOL HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals NY LLC)
The FDA approved a supplemental application for propranolol hydrochloride from Amneal Pharmaceuticals NY LLC, signifying approval of a gener…
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FDA approval · 2008-02-21FDA Approved: ISOSORBIDE DINITRATE — Supplemental Application (Sandoz Inc.)
FDA has approved a supplemental application for Isosorbide Dinitrate by Sandoz Inc., indicating a regulatory update for this generic product…
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FDA approval · 2008-02-21FDA Approved: ISOSORBIDE DINITRATE — Supplemental Application (Sandoz Inc.)
The FDA approved a supplemental application for Sandoz Inc.'s isosorbide dinitrate product.
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FDA approval · 2008-02-19FDA Approved: AMLODIPINE BESYLATE — Supplemental Application (Zydus Pharmaceuticals USA Inc.)
FDA approved a supplemental application for amlodipine besylate by Zydus Pharmaceuticals USA Inc. under the ANDA framework. The action relat…
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CLINICAL_TRIALS trial_result · 2008-02-15Clinical Trial Update: Copenhagen Arterial Revascularization Randomized Patency and Outcome Trial [Phase 3]
Phase 3 randomized trial investigating arterial revascularization for coronary arteriosclerosis and ischemic heart disease; the status of th…
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FDA approval · 2008-01-31FDA Approved: PROPRANOLOL HYDROCHLORIDE — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a generic version of propranolol hydrochloride for the same indications as the brand product, enabling generic competition for …
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CLINICAL_TRIALS trial_result · 2008-01-29Clinical Trial Update: Stem Cell Study for Patients With Heart Disease [Phase 1]
Phase 1 stem cell study in patients with ischemic heart disease has completed its Phase 1 status, with endpoints related to myocardial ische…
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FDA approval · 2008-01-08FDA Approved: LOPRESSOR — Supplemental Application (Validus Pharmaceuticals LLC)
FDA approved a supplemental application for Lopressor (metoprolol tartrate) filed by Validus Pharmaceuticals LLC.
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FDA approval · 2008-01-07FDA Approved: PROPRANOLOL HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals NY LLC)
FDA approved a supplemental application for propranolol hydrochloride from Amneal Pharmaceuticals NY LLC.
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FDA approval · 2007-12-13FDA Approved: BISOPROLOL FUMARATE — Supplemental Application (NorthStar Rx LLC)
FDA approved a supplemental application for Bisoprolol fumarate (NorthStar Rx LLC), granting supplemental approval for this generic product.
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FDA label_change · 2007-10-31FDA Approved: NORVASC — Supplemental Application (Viatris Specialty LLC)
The FDA approved a supplemental application for NORVASC (amlodipine besylate) by Viatris Specialty LLC, resulting in changes to the labeling…
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FDA approval · 2007-10-31FDA Approved: ATENOLOL — Original Application (Aurobindo Pharma Limited)
FDA approved Atenolol from Aurobindo Pharma Limited under an Original Application (ANDA) for a generic beta-blocker.
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FDA approval · 2007-09-26FDA Approved: AMLODIPINE BESYLATE — Original Application (Cipla USA Inc.)
The FDA approved Cipla USA Inc.'s original application for amlodipine besylate, a generic version of the calcium channel blocker used to tre…
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FDA approval · 2007-09-11FDA Approved: METOPROLOL TARTRATE — Original Application (Aurobindo Pharma Limited)
FDA approved metoprolol tartrate as an original application generic product for Aurobindo Pharma Limited.
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FDA approval · 2007-09-05FDA Approved: CARVEDILOL — Original Application (Dr. Reddy's Laboratories Limited)
FDA approved Carvedilol on an original application by Dr. Reddy's Laboratories Limited (generic carvedilol).
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CLINICAL_TRIALS trial_result · 2007-09-03Clinical Trial Update: Vescell(TM) for the Treatment of Patients With Severe Anginal Syndrome With or Without Heart Failure [Phase 1, Phase 2]
This entry notes a Phase 1/2 clinical trial evaluating Vescell for severe anginal syndrome with or without heart failure, with an unknown st…
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FDA approval · 2007-08-28FDA Approved: AMLODIPINE BESYLATE — Original Application (Cipla USA Inc.)
FDA approved Cipla USA Inc.'s original application for amlodipine besylate, a generic calcium channel blocker used to treat hypertension and…
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FDA approval · 2007-08-10FDA Approved: PROPRANOLOL HYDROCHLORIDE — Original Application (Actavis Pharma, Inc.)
The FDA approved Actavis Pharma's generic propranolol hydrochloride product in an Original ANDA submission.
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FDA approval · 2007-07-12FDA Approved: AMLODIPINE BESYLATE — Original Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' original application for amlodipine besylate (generic), enabling the marketing of a generic calcium chan…