Hypertension
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Sign up freeTop drugs studied for this disease
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FDA approval · 2021-12-20FDA Approved: IRBESARTAN — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)
The FDA approved a supplemental application for IRBESARTAN from Unichem Pharmaceuticals (USA), Inc. for this generic product (ANDA 203020).
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FDA approval · 2021-12-17FDA Approved: NEBIVOLOL — Original Application (Modavar Pharmaceuticals LLC)
FDA approved the original abbreviated new drug application for Nebivolol by Modavar Pharmaceuticals LLC, establishing a generic version of n…
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FDA approval · 2021-12-17FDA Approved: NEBIVOLOL — Original Application (Aurobindo Pharma Limited)
FDA approved Nebivolol via an original Abbreviated New Drug Application by Aurobindo Pharma Limited.
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FDA approval · 2021-12-08FDA Approved: IRBESARTAN — Supplemental Application (NorthStar RxLLC)
The FDA approved a supplemental application for irbesartan from NorthStar RxLLC, authorizing changes to an existing generic product under an…
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FDA approval · 2021-12-08FDA Approved: IRBESARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved a supplemental application for Irbesartan and Hydrochlorothiazide from Unichem Pharmaceuticals (USA), Inc. to support the comme…
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FDA approval · 2021-12-06FDA Approved: VALSARTAN — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for valsartan submitted by Aurobindo Pharma Limited, updating the existing approval for this generic…
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FDA approval · 2021-12-06FDA Approved: VALSARTAN — Supplemental Application (Macleods Pharmaceuticals Limited)
FDA approved a supplemental application for VALSARTAN from Macleods Pharmaceuticals Limited. This approval supports continued distribution o…
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FDA approval · 2021-12-03FDA Approved: IRBESARTAN — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved a supplemental application for irbesartan submitted by Lupin Pharmaceuticals, Inc.
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FDA approval · 2021-11-19FDA Approved: NEBIVOLOL — Supplemental Application (Ascend Laboratories, LLC)
The FDA approved a supplemental application for Nebivolol from Ascend Laboratories, LLC (ANDA 203828).
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FDA approval · 2021-11-09FDA Approved: PROCARDIA XL — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
The FDA approved a supplemental application for Procardia XL (nifedipine) from Pfizer Laboratories Div Pfizer Inc, updating the drug's label…
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FDA approval · 2021-11-08FDA Approved: METOPROLOL SUCCINATE — Supplemental Application (Epic Pharma, LLC)
FDA approved a supplemental application for a generic metoprolol succinate product from Epic Pharma, LLC.
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FDA approval · 2021-11-04FDA Approved: BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE — Original Application (ANI Pharmaceuticals, Inc.)
FDA approved ANI Pharmaceuticals' generic fixed-dose combination tablet of bisoprolol fumarate and hydrochlorothiazide for hypertension.
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FDA approval · 2021-11-02FDA Approved: VALSARTAN — Original Application (ANI Pharmaceuticals, Inc.)
The FDA approved ANI Pharmaceuticals' original ANDA for valsartan, enabling generic manufacture and marketing of valsartan for its approved …
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FDA approval · 2021-10-27FDA Approved: VALSARTAN — Original Application (ScieGen Pharmaceuticals, INC.)
FDA approves the original application for VALSARTAN (Valsartan) from ScieGen Pharmaceuticals as a generic angiotensin II receptor blocker. I…
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EMA approval · 2021-10-26EMA Authorised: Telmisartan Teva Pharma (telmisartan) — Teva B.V.
The EMA authorised Telmisartan Teva Pharma (telmisartan) for hypertension, with Teva B.V. as the marketing authorization holder.
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FDA approval · 2021-10-25FDA Approved: METOPROLOL TARTRATE — Supplemental Application (Hospira, Inc.)
FDA approved Hospira's supplemental application for metoprolol tartrate (generic beta-blocker), under an ANDA.
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FDA approval · 2021-10-25FDA Approved: EPLERENONE — Original Application (Westminster Pharmaceuticals, LLC)
FDA approves Westminster Pharmaceuticals' original ANDA for EPLERENONE (generic eplerenone), providing a generic option for hypertension and…
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FDA approval · 2021-10-25FDA Approved: ATENOLOL AND CHLORTHALIDONE — Original Application (MARLEX PHARMACEUTICALS, INC)
FDA approved Atenolol and Chlorthalidone tablets as an Original Application under an ANDA from Marlex Pharmaceuticals, for the treatment of …
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FDA approval · 2021-10-15FDA Approved: TELMISARTAN — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
The FDA approved a supplemental application for telmisartan from Glenmark Pharmaceuticals Inc., USA, resulting in updated labeling for the d…
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FDA approval · 2021-10-05FDA Approved: VALSARTAN — Original Application (Dr. Reddy's Laboratories Limited)
FDA approves the original application for valsartan from Dr. Reddy's Laboratories Limited, granting approval for the generic product.
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FDA approval · 2021-10-01FDA Approved: RAMIPRIL — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for Ramipril from Rising Pharma Holdings, Inc., enabling the continued manufacture and distribut…
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FDA approval · 2021-09-15FDA Approved: IRBESARTAN — Supplemental Application (Solco Healthcare U.S., LLC)
FDA approved a supplemental application for IRBESARTAN from Solco Healthcare U.S., LLC.
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FDA approval · 2021-09-14FDA Approved: IRBESARTAN — Supplemental Application (Lupin Pharmaceuticals, Inc.)
The FDA approved Lupin Pharmaceuticals' supplemental application for IRBESARTAN, a generic angiotensin II receptor blocker.
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FDA approval · 2021-09-13FDA Approved: KATERZIA — Supplemental Application (Azurity Pharmaceuticals, Inc.)
FDA approved a supplemental application for KATERZIA (amlodipine) from Azurity Pharmaceuticals, Inc., expanding the approved labeling/formul…
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FDA approval · 2021-09-01FDA Approved: IRBESARTAN — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for IRBESARTAN from Aurobindo Pharma Limited under ANDA 203081.