Benign Prostatic Hyperplasia
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Sign up freeTop drugs studied for this disease
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FDA approval · 2020-02-14FDA Approved: SILODOSIN — Original Application (Camber Pharmaceuticals, Inc.)
FDA approved Camber Pharmaceuticals' original application for generic silodosin for the treatment of signs and symptoms of benign prostatic …
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FDA approval · 2019-11-22FDA Approved: SILODOSIN — Original Application (Alembic Pharmaceuticals Limited)
FDA approved the original ANDA for silodosin submitted by Alembic Pharmaceuticals Limited, establishing a generic version of silodosin for t…
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FDA approval · 2019-10-16FDA Approved: TADALAFIL — Original Application (Macleods Pharmaceuticals Limited)
FDA approved Macleods Pharmaceuticals Limited's original ANDA for tadalafil, enabling a generic version of the medication.
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FDA approval · 2019-10-07FDA Approved: TADALAFIL — Original Application (Macleods Pharmaceuticals Limited)
The FDA approved Macleods Pharmaceuticals Limited's original application for tadalafil (TADALAFIL) as a generic product.
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FDA approval · 2019-09-23FDA Approved: TAMSULOSIN HYDROCHLORIDE — Supplemental Application (Ascend Laboratories, LLC)
The FDA approved a supplemental application for tamsulosin hydrochloride submitted by Ascend Laboratories, LLC.
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FDA approval · 2019-09-23FDA Approved: TAMSULOSIN HYDROCHLORIDE — Supplemental Application (Macleods Pharmaceuticals Limited)
The FDA approved a supplemental application for tamsulosin hydrochloride submitted by Macleods Pharmaceuticals Limited. The approval relates…
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FDA approval · 2019-09-09FDA Approved: TAMSULOSIN HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for tamsulosin hydrochloride submitted by Sun Pharmaceutical Industries, Inc.
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FDA approval · 2019-09-09FDA Approved: TAMSULOSIN HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for tamsulosin hydrochloride from Aurobindo Pharma Limited.
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FDA approval · 2019-09-09FDA Approved: TAMSULOSIN HYDROCHLORIDE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for tamsulosin hydrochloride by Zydus Lifesciences Limited, enabling the generic product to be marke…
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FDA approval · 2019-03-29FDA Approved: TADALAFIL — Original Application (Teva Pharmaceuticals, Inc.)
FDA approved Teva's tadalafil generic (ANDA 205885) under Original Application. The product is indicated for erectile dysfunction and benign…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approved Amneal's generic tadalafil tablets under an original ANDA, making a generic tadalafil available for erectile dysfunction and be…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Quallent Pharmaceuticals Health LLC)
FDA approved an Original Application (ANDA) for tadalafil submitted by Quallent Pharmaceuticals Health LLC.
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Zydus Pharmaceuticals USA Inc.)
FDA approves Zydus Pharmaceuticals USA Inc.'s generic tadalafil (TADALAFIL) for Erectile Dysfunction and Benign Prostatic Hyperplasia under …
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Torrent Pharmaceuticals Limited)
The FDA approved Torrent Pharmaceuticals Limited's original application for tadalafil as a generic drug. The approval covers indications for…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Aurobindo Pharma Limited)
The FDA approved the original ANDA for tadalafil from Aurobindo Pharma Limited, enabling a generic version of tadalafil to be marketed in th…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved the original application for tadalafil from Unichem Pharmaceuticals (USA), Inc., authorizing a generic tadalafil product for th…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (NorthStar RxLLC)
FDA approved a tadalafil generic by NorthStar RxLLC via an Original Application (ANDA208934) for erectile dysfunction and benign prostatic h…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Dr.Reddys Laboratories Inc)
FDA approved Dr. Reddy's Laboratories' original application for tadalafil, a generic version of the erectile dysfunction medication Cialis.
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Qilu Pharmaceutical Co., Ltd.)
FDA approved a generic tadalafil (TADALAFIL) from Qilu Pharmaceutical Co., Ltd. under an original ANDA.
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (HEC Pharm USA Inc.)
FDA approves the original ANDA for tadalafil by HEC Pharm USA Inc., enabling a generic tadalafil product. It covers indications commonly ass…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Alembic Pharmaceuticals Inc.)
FDA approved Alembic Pharmaceuticals' original application for generic tadalafil (Tadalafil) for erectile dysfunction and benign prostatic h…
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Torrent Pharmaceuticals Limited)
FDA approved Torrent Pharmaceuticals Limited's generic tadalafil tablet under an Original Application (ANDA).
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FDA approval · 2019-03-26FDA Approved: TADALAFIL — Original Application (Camber Pharmaceuticals, Inc.)
FDA approved Camber Pharmaceuticals' generic tadalafil under an Original Application (ANDA 209908). The approval covers tadalafil for erecti…
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FDA approval · 2019-02-05FDA Approved: TADALAFIL — Original Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' generic tadalafil under an Original Application (ANDA), enabling a new generic version of tadalafil for …
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FDA approval · 2019-02-05FDA Approved: TADALAFIL — Original Application (Quallent Pharmaceuticals Health LLC)
FDA approved the original application for tadalafil by Quallent Pharmaceuticals Health LLC, making the first generic tadalafil available for…