Seasonal Affective Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2022-01-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for bupropion hydrochloride from Sun Pharmaceutical Industries, authorizing the generic product’s ma…
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FDA approval · 2022-01-03FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Slate Run Pharmaceuticals, LLC)
The FDA approved a supplemental application for Bupropion Hydrochloride XL from Slate Run Pharmaceuticals, LLC.
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FDA approval · 2021-12-13FDA Approved: BUPROPION HYDROCHLORIDE (SR) — Supplemental Application (ScieGen Pharmaceuticals, Inc.)
FDA approved ScieGen Pharmaceuticals' supplemental application for a sustained-release generic version of bupropion hydrochloride, with the …
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FDA approval · 2021-03-12FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Solco Healthcare US LLC)
The FDA approved a supplemental application for a generic version of Bupropion hydrochloride sustained-release from Solco Healthcare US LLC …
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FDA approval · 2021-01-04FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for Bupropion Hydrochloride from Amneal Pharmaceuticals of New York LLC, authorizing the generic pro…
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FDA approval · 2021-01-04FDA Approved: BUPROPION HYDROCHLORIDE (SR) — Supplemental Application (Cipla USA Inc.,)
The FDA approved Cipla USA Inc.'s supplemental application for Bupropion hydrochloride sustained-release, enabling the generic product to be…
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FDA approval · 2020-12-31FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approves Sun Pharmaceutical's generic bupropion hydrochloride under an Original Application (ANDA).
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FDA approval · 2020-12-22FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Dr. Reddys Laboratories Inc.)
The FDA approved a supplemental application for Bupropion Hydrochloride SR, granting approval for the generic sustained-release formulation …
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FDA approval · 2020-12-21FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for bupropion hydrochloride by Aurobindo Pharma Limited.
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FDA approval · 2020-12-21FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Slate Run Pharmaceuticals, LLC)
The FDA approved a supplemental application for Bupropion hydrochloride sustained-release by Slate Run Pharmaceuticals, LLC.
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FDA approval · 2020-11-30FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical Industries' generic Bupropion hydrochloride under an original application.
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FDA approval · 2020-10-29FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (CIPLA USA INC.,)
FDA approved a supplemental application for BUPROPION HYDROCHLORIDE from CIPLA USA INC., updating the existing approved product.
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FDA approval · 2020-10-16FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for BUPROPION HYDROCHLORIDE XL by Actavis Pharma, Inc. under the ANDA process for the extended-relea…
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FDA approval · 2020-10-07FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
The FDA approved a supplemental application for bupropion hydrochloride from Actavis Pharma, Inc., indicating an approved change to the gene…
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FDA approval · 2020-09-28FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Slate Run Pharmaceuticals, LLC)
FDA approves a supplemental application for Bupropion Hydrochloride Sustained-Release, submitted by Slate Run Pharmaceuticals, LLC.
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FDA approval · 2020-07-10FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' supplemental application for a generic Bupropion Hydrochloride Extended-Release (XL) product.
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FDA approval · 2020-06-30FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for Bupropion Hydrochloride from Rising Pharma Holdings, Inc., for a generic product under an AN…
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FDA approval · 2020-06-30FDA Approved: BUPROPION HYDROCHLORIDE (XL) — Supplemental Application (Exelan Pharmaceuticals Inc.)
FDA approved a supplemental application for bupropion hydrochloride extended-release (XL) from Exelan Pharmaceuticals Inc., enabling continu…
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FDA approval · 2020-03-05FDA Approved: BUPROPION — Supplemental Application (Zydus Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for Bupropion by Zydus Pharmaceuticals USA Inc.
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FDA approval · 2020-01-16FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Cadila Pharmaceuticals Limited)
FDA approved bupropion hydrochloride as a generic under Cadila Pharmaceuticals Limited's original ANDA.
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FDA approval · 2019-12-10FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Upsher-Smith Laboratories, LLC)
The FDA approved Upsher-Smith Laboratories' supplemental application for bupropion hydrochloride, updating the product labeling.
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FDA approval · 2019-11-05FDA Approved: WELLBUTRIN XL — Supplemental Application (Bausch Health US LLC)
The FDA approved a supplemental application for WELLBUTRIN XL (bupropion hydrochloride) submitted by Bausch Health US LLC under NDA021515.
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FDA approval · 2019-09-05FDA Approved: BUPROPION HYDROCHLORIDE XL — Original Application (Oryza pharmaceuticals Inc.)
FDA approved a generic version of bupropion hydrochloride extended-release (XL) from Oryza Pharmaceuticals Inc. under an original applicatio…
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FDA approval · 2019-01-28FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Rising Pharma Holdings, Inc.)
FDA approved an original application for bupropion hydrochloride as a generic drug. The approval was issued to Rising Pharma Holdings, Inc.
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FDA approval · 2019-01-24FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals, Inc.'s generic Bupropion Hydrochloride XL as an extended-release antidepressant under an ANDA supplement…