Hypertension
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Sign up freeTop drugs studied for this disease
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FDA approval · 2022-06-30FDA Approved: RAMIPRIL — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for ramipril submitted by Zydus Lifesciences Limited under ANDA078832.
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FDA approval · 2022-06-29FDA Approved: ENALAPRIL MALEATE — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approves the original generic application for enalapril maleate (Enalapril) manufactured by Amneal Pharmaceuticals NY LLC.
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FDA approval · 2022-06-28FDA Approved: OLMESARTAN MEDOXOMIL — Supplemental Application (QUALLENT PHARMACEUTICALS HEALTH LLC)
FDA approved a supplemental application for olmesartan medoxomil filed by Quallent Pharmaceuticals Health LLC.
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FDA approval · 2022-06-27FDA Approved: OLMESARTAN MEDOXOMIL — Supplemental Application (Alembic Pharmaceuticals Inc.)
FDA approved a supplemental application for olmesartan medoxomil submitted by Alembic Pharmaceuticals Inc.
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FDA approval · 2022-06-15FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Lifestar Pharma LLC)
FDA approves a generic Verapamil Hydrochloride product from Lifestar Pharma LLC under an Original Application (ANDA).
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FDA approval · 2022-06-08FDA Approved: GUANFACINE HYDROCHLORIDE — Original Application (TWi Pharmaceuticals, Inc.)
FDA approved guanfacine hydrochloride as an Original Application (ANDA) submission by TWi Pharmaceuticals, Inc., establishing a generic vers…
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FDA approval · 2022-06-07FDA Approved: NADOLOL — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for Nadolol submitted by Aurobindo Pharma Limited under the ANDA, approving updated labeling for…
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FDA approval · 2022-06-01FDA Approved: TOPROL XL — Supplemental Application (Melinta Therapeutics, LLC)
The FDA approved a supplemental application for TOPROL XL (metoprolol succinate) submitted by Melinta Therapeutics, LLC. This action updates…
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FDA approval · 2022-05-27FDA Approved: ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE — Supplemental Application (Taro Pharmaceuticals U.S.A., Inc.)
FDA approved a supplemental application for Enalapril Maleate and Hydrochlorothiazide (a fixed-dose combination) by Taro Pharmaceuticals U.S…
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FDA approval · 2022-05-27FDA Approved: QUINAPRIL HCL AND HYDROCHLOROTHIAZIDE — Supplemental Application (Lupin Pharmaceuticals,Inc.)
The FDA approved Lupin Pharmaceuticals' supplemental application for Quinapril HCl and Hydrochlorothiazide, a fixed-dose combination for the…
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FDA approval · 2022-05-26FDA Approved: QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for Quinapril hydrochloride/hydrochlorothiazide from Aurobindo Pharma Limited, enabling the mark…
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FDA approval · 2022-05-25FDA Approved: QUINAPRIL AND HYDROCHLOROTHIAZIDE 10/12.5 — Supplemental Application (Cipla USA Inc.)
The FDA approved Cipla USA Inc.'s supplemental application for Quinapril and Hydrochlorothiazide in strengths 10/12.5, 20/12.5, and 20/25.
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FDA approval · 2022-05-05FDA Approved: DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE — Original Application (Dr. Reddy's Labratories Inc.)
FDA approves Dr. Reddy's Laboratories' generic diltiazem hydrochloride extended-release tablet (ANDA 215775).
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FDA approval · 2022-04-26FDA Approved: NIFEDIPINE — Supplemental Application (Ascend Laboratories, LLC)
The FDA approved a supplemental application for nifedipine from Ascend Laboratories, LLC, under the existing ANDA, authorizing changes to an…
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FDA approval · 2022-04-12FDA Approved: FUROSEMIDE — Supplemental Application (Phlow Corporation)
FDA granted a supplemental approval for Furosemide by Phlow Corporation under the existing NDA; the snippet does not specify the exact natur…
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FDA approval · 2022-04-07FDA Approved: NEBIVOLOL — Original Application (Solco Healthcare US, LLC)
The FDA approved the original application for Nebivolol (generic) from Solco Healthcare US, LLC. Nebivolol is used to treat hypertension.
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FDA approval · 2022-04-05FDA Approved: IRBESARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for the irbesartan and hydrochlorothiazide product from Hikma Pharmaceuticals USA, updating labeling…
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FDA approval · 2022-04-05FDA Approved: IRBESARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Macleods Pharmaceuticals Limited)
FDA approved a supplemental application for Macleods' irbesartan/hydrochlorothiazide combination tablet, expanding its labeling for the trea…
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FDA approval · 2022-04-04FDA Approved: VALSARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for a generic fixed-dose combination of valsartan and hydrochlorothiazide by Aurobindo Pharma Limite…
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FDA approval · 2022-03-31FDA Approved: QUINAPRIL — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for a quinapril hydrochloride generic product manufactured by Aurobindo Pharma Limited.
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FDA approval · 2022-03-30FDA Approved: ENALAPRIL MALEATE ORAL SOLUTION — Original Application (Ascend Laboratories, LLC)
The FDA approved Ascend Laboratories' enalapril maleate oral solution as an original generic application for enalapril; the drug is used to …
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FDA approval · 2022-03-29FDA Approved: NIFEDIPINE — Original Application (Ascend Laboratories, LLC)
FDA approved Ascend Laboratories' Original Application for nifedipine, a calcium channel blocker used to treat hypertension and angina.
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FDA approval · 2022-03-21FDA Approved: ESMOLOL HYDROCHLORIDE — Original Application (Eugia US LLC)
FDA approved the original application for esmolol hydrochloride in sodium chloride injection, a generic product manufactured by Eugia US LLC…
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FDA approval · 2022-03-17FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved the original Abbreviated New Drug Application for verapamil hydrochloride from Heritage Pharmaceuticals (d/b/a Avet) as a gener…
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FDA approval · 2022-03-15FDA Approved: NEBIVOLOL HYDROCHLORIDE — Original Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved Nebivolol hydrochloride as an original generic application (ANDA) from Unichem Pharmaceuticals (USA), Inc. for hypertension.