Pain
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Sign up freeTop drugs studied for this disease
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FDA approval · 2017-05-26FDA Approved: MORPHINE SULFATE EXTENDED RELEASE — Supplemental Application (Rhodes Pharmaceuticals L. P.)
The FDA approved a supplemental application for Morphine Sulfate Extended Release from Rhodes Pharmaceuticals L. P., authorizing continued m…
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FDA approval · 2017-05-26FDA Approved: MORPHINE SULFATE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Morphine Sulfate from Actavis Pharma, Inc., permitting continued marketing of the generic produc…
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FDA approval · 2017-05-26FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Epic Pharma, LLC)
FDA approved a supplemental application for methadone hydrochloride from Epic Pharma, LLC, approving the generic formulation.
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FDA approval · 2017-05-26FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for Methadone Hydrochloride by Hikma Pharmaceuticals USA Inc., updating the product's approved i…
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FDA approval · 2017-05-26FDA Approved: MORPHINE SULFATE — Supplemental Application (Actavis Pharma, Inc.)
The FDA approved a supplemental application for Morphine Sulfate submitted by Actavis Pharma, Inc.
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FDA approval · 2017-05-26FDA Approved: XTAMPZA ER — Supplemental Application (Collegium Pharmaceutical, Inc.)
FDA approved a supplemental application for XTAMPZA ER (oxycodone) from Collegium Pharmaceutical, Inc. The approval authorizes changes under…
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FDA approval · 2017-05-26FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc., documenting the acceptance of a sup…
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FDA approval · 2017-05-26FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc. to modify/update the product's appro…
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FDA approval · 2017-05-23FDA Approved: BUPRENORPHINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for buprenorphine by Sun Pharmaceutical Industries, Inc., through an ANDA supplement to modify or ad…
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FDA approval · 2017-05-23FDA Approved: BUPRENORPHINE — Supplemental Application (Rhodes Pharmaceuticals L.P.)
FDA approved a supplemental application for buprenorphine from Rhodes Pharmaceuticals L.P., indicating regulatory action on an existing prod…
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FDA approval · 2017-05-23FDA Approved: BUPRENORPHINE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved Hikma Pharmaceuticals USA Inc.'s supplemental application for buprenorphine (generic), marking regulatory approval for the gene…
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FDA approval · 2017-05-19FDA Approved: MORPHINE SULFATE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for Morphine Sulfate by Amneal Pharmaceuticals of New York LLC under ANDA 200411, granting a supplem…
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FDA approval · 2017-04-20FDA Approved: PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE — Supplemental Application (Lupin Pharmaceuticals,Inc.)
FDA approved Lupin's supplemental application for Pentazocine Hydrochloride and Naloxone Hydrochloride, updating the product's approval unde…
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FDA approval · 2017-04-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
FDA approved a supplemental application for Hydrocodone Bitartrate and Acetaminophen from Rhodes Pharmaceuticals L.P., expanding the approve…
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FDA approval · 2017-03-31FDA Approved: PENTAZOCINE AND NALOXONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for Pentazocine and Naloxone from Sun Pharmaceutical Industries, Inc.
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FDA approval · 2017-03-31FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Original Application (SpecGx LLC)
FDA approved Hydrocodone Bitartrate and Acetaminophen as an original generic application from SpecGx LLC.
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FDA approval · 2017-03-27FDA Approved: BUPRENORPHINE — Original Application (Rhodes Pharmaceuticals L.P.)
FDA approves Rhodes Pharmaceuticals L.P.'s original ANDA application for a generic buprenorphine product.
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FDA approval · 2017-03-22FDA Approved: OXYCODONE AND ACETAMINOPHEN — Original Application (Camber Pharmaceuticals, Inc.)
FDA approved Camber Pharmaceuticals' original application for a generic oxycodone/acetaminophen product.
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FDA approval · 2017-03-16FDA Approved: INFANTS MOTRIN — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for INFANTS MOTRIN (ibuprofen) submitted by Kenvue Brands LLC, related to changes to the product…
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FDA approval · 2017-03-10FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc., approving the generic product's sup…
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FDA approval · 2017-02-10FDA Approved: OXYCODONE AND ACETAMINOPHEN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
The FDA approved Rhodes Pharmaceuticals L.P.'s supplemental application for Oxycodone and Acetaminophen, a fixed-dose opioid analgesic.
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FDA approval · 2017-01-23FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (VistaPharm, LLC)
FDA approved a supplemental application for methadone hydrochloride from VistaPharm, LLC under the ANDA pathway.
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FDA approval · 2016-12-16FDA Approved: DISKETS — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for DISKETS (methadone hydrochloride) from Hikma Pharmaceuticals USA Inc., reflecting an approved su…
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FDA approval · 2016-12-16FDA Approved: MS CONTIN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
The FDA approved a supplemental application for MS CONTIN (morphine sulfate) submitted by Rhodes Pharmaceuticals L.P. This action confirms t…
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FDA approval · 2016-12-16FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc., finalizing the approval of a generi…