Alcohol Withdrawal Syndrome
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Sign up freeTop drugs studied for this disease
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FDA approval · 2021-02-05FDA Approved: DIAZEPAM INTENSOL — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for Diazepam Intensol from Hikma Pharmaceuticals USA Inc.
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FDA approval · 2021-02-05FDA Approved: DIAZEPAM — Supplemental Application (Hospira, Inc.)
FDA approved a supplemental application for diazepam from Hospira, Inc., under an ANDA, indicating regulatory approval of the requested chan…
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FDA approval · 2021-02-05FDA Approved: DIAZEPAM — Supplemental Application (Meridian Medical Technologies LLC)
The FDA approved a supplemental application for Diazepam submitted by Meridian Medical Technologies LLC.
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FDA approval · 2021-02-05FDA Approved: CHLORDIAZEPOXIDE HYDROCHLORIDE — Supplemental Application (Epic Pharma, LLC)
The FDA approved a supplemental application for chlordiazep oxide hydrochloride from Epic Pharma, LLC.
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FDA approval · 2021-02-05FDA Approved: DIAZEPAM — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for diazepam from Hikma Pharmaceuticals USA Inc. to market a generic diazepam product.
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FDA approval · 2021-02-05FDA Approved: CHLORDIAZEPOXIDE HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
FDA approved a supplemental application for chlordiazepoxide hydrochloride by Epic Pharma LLC, indicating a regulatory modification to an ap…
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FDA approval · 2021-02-05FDA Approved: DIAZEPAM — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved Hikma Pharmaceuticals USA Inc.'s supplemental application for Diazepam, approving a generic version of the drug.
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FDA approval · 2020-08-17FDA Approved: DIAZEPAM — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for diazepam from Hikma Pharmaceuticals USA Inc., updating the approved product under the existi…
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FDA approval · 2019-12-26FDA Approved: DIAZEPAM — Original Application (Natco Pharma USA LLC)
FDA approved Natco Pharma USA LLC's original application for a generic diazepam product, enabling its marketing in the United States.
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FDA approval · 2019-11-06FDA Approved: DIAZEPAM — Supplemental Application (Natco Pharma USA LLC)
The FDA approved a supplemental application for Diazepam from Natco Pharma USA LLC, granting approval of generic diazepam under ANDA210363.
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FDA approval · 2019-02-21FDA Approved: DIAZEPAM — Supplemental Application (Hospira, Inc.)
FDA approved a supplemental application for Diazepam filed by Hospira, Inc. (ANDA 072079).
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FDA approval · 2019-02-21FDA Approved: DIAZEPAM — Supplemental Application (Hospira, Inc.)
The FDA approved a supplemental application for diazepam from Hospira, Inc., indicating updated labeling and continued availability under th…
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FDA approval · 2016-12-16FDA Approved: DIAZEPAM — Supplemental Application (Oceanside Pharmaceuticals)
FDA approved a supplemental application for Diazepam from Oceanside Pharmaceuticals, resulting in changes to the drug's labeling.
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FDA approval · 2016-12-16FDA Approved: CHLORDIAZEPOXIDE HYDROCHLORIDE — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for chlordiazepoxide hydrochloride (generic) from Chartwell RX, LLC, updating the approval of this g…
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FDA approval · 2016-12-16FDA Approved: CHLORDIAZEPOXIDE HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
The FDA approved a supplemental application for chlordiazepoxide hydrochloride from Epic Pharma LLC, confirming regulatory clearance for a g…
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FDA approval · 2016-12-16FDA Approved: CHLORDIAZEPOXIDE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva's supplemental application for chlordiazepoxide hydrochloride, authorizing changes to the approved product (such as la…
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FDA approval · 2016-06-24FDA Approved: DIAZEPAM — Original Application (Chartwell Governmental & Specialty RX, LLC.)
FDA approved the original application for diazepam oral from Chartwell Governmental & Specialty RX, LLC. This marks approval of a generic di…
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FDA approval · 2016-05-02FDA Approved: DIAZEPAM INTENSOL — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for Diazepam Intensol from Hikma Pharmaceuticals USA Inc., confirming changes to the approved pr…
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FDA approval · 2016-03-24FDA Approved: DIAZEPAM — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application to Chartwell RX, LLC for diazepam oral solution (concentrate), authorizing a generic version of this…
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FDA approval · 2015-04-06FDA Approved: DIAZEPAM — Supplemental Application (Hospira, Inc.)
The FDA approved Hospira, Inc.'s supplemental application for diazepam (generic) under the ANDA.
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FDA approval · 2015-03-09FDA Approved: DIAZEPAM — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a Teva supplemental application for Diazepam, resulting in an approved labeling change under ANDA 071321.
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FDA approval · 2014-04-14FDA Approved: DIAZEPAM — Original Application (Chartwell RX, LLC)
FDA approved Chartwell RX, LLC's original application for diazepam oral solution (concentrate) as a generic product.
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FDA approval · 2013-01-28FDA Approved: DIAZEPAM — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for diazepam from Teva Pharmaceuticals USA, Inc. The action represents an additional approval or mod…
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FDA approval · 2012-09-13FDA Approved: LORAZEPAM — Supplemental Application (International Medication Systems, Limited)
FDA approved a supplemental application for lorazepam from International Medication Systems, Limited.
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FDA approval · 2010-01-20FDA Approved: CLORAZEPATE DIPOTASSIUM — Supplemental Application (NORTHSTAR RX LLC)
The FDA approved a supplemental application for clorazepate dipotassium submitted by Northstar RX LLC.