Pain
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Sign up freeTop drugs studied for this disease
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FDA approval · 2016-09-30FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (VistaPharm, LLC)
FDA approved a supplemental application for a generic methadone hydrochloride product from VistaPharm, LLC. The drug is used for opioid use …
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FDA approval · 2016-09-30FDA Approved: TAPENTADOL — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for Tapentadol hydrochloride submitted by Hikma Pharmaceuticals USA Inc.
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FDA approval · 2016-09-30FDA Approved: MORPHINE SULFATE EXTENDED RELEASE — Supplemental Application (Rhodes Pharmaceuticals L. P.)
FDA approved a supplemental application for Morphine Sulfate Extended Release from Rhodes Pharmaceuticals L.P., approving changes under a su…
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FDA approval · 2016-09-30FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Aurolife Pharma, LLC)
FDA approved a supplemental application for methadone hydrochloride from Aurolife Pharma, LLC, making a generic version of the drug availabl…
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FDA approval · 2016-09-30FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Epic Pharma, LLC)
FDA approved a supplemental application for methadone hydrochloride from Epic Pharma, LLC.
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FDA approval · 2016-09-30FDA Approved: XTAMPZA ER — Supplemental Application (Collegium Pharmaceutical, Inc.)
The FDA approved a supplemental application for XTAMPZA ER (oxycodone) from Collegium Pharmaceutical, Inc., likely updating labeling or indi…
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FDA approval · 2016-09-30FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Ascend Laboratories, LLC)
FDA approved a supplemental application for a generic methadone hydrochloride product from Ascend Laboratories, LLC.
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FDA approval · 2016-09-02FDA Approved: DICLOFENAC SODIUM — Original Application (SOLA Pharmaceuticals, LLC)
FDA approved SOLA Pharmaceuticals' diclofenac sodium tablet as an original generic, indicated for relief of pain and inflammation in conditi…
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FDA approval · 2016-07-07FDA Approved: BUPRENORPHINE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for buprenorphine (generic) filed by Hikma Pharmaceuticals USA Inc.; this covers an update to the ap…
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FDA approval · 2016-07-07FDA Approved: BUPRENORPHINE HYDROCHLORIDE — Supplemental Application (PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma)
FDA approved a supplemental application for buprenorphine hydrochloride (generic) from PAI Holdings, under ANDA 090622.
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FDA approval · 2016-07-07FDA Approved: HYDROMORPHONE HYDROCHLORIDE — Original Application (Trigen Laboratories, LLC)
FDA approved Hydromorphone Hydrochloride as a generic drug under an Original Application (ANDA205629) from Trigen Laboratories, LLC for the …
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FDA approval · 2016-06-15FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Original Application (Strides Pharma Science Limited)
FDA approved Strides Pharma Science Limited's generic hydrocodone bitartrate and acetaminophen tablet for short-term relief of moderate to s…
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FDA approval · 2016-05-09FDA Approved: DICLOFENAC SODIUM — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for diclofenac sodium from Aurobindo Pharma Limited.
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FDA approval · 2016-05-09FDA Approved: KETOROLAC TROMETHAMINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for ketorolac tromethamine (Sun Pharmaceutical Industries, Inc.) under an ANDA.
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FDA approval · 2016-05-09FDA Approved: SPRIX — Supplemental Application (Zyla Life Sciences US LLC)
The FDA approved a supplemental application for SPRIX (ketorolac tromethamine) submitted by Zyla Life Sciences US LLC.
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FDA approval · 2016-05-09FDA Approved: KETOROLAC TROMETHAMINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for ketorolac tromethamine from Teva Pharmaceuticals USA, Inc., indicating an approved modification …
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FDA approval · 2016-05-09FDA Approved: KETOROLAC TROMETHAMINE — Supplemental Application (Onesource Specialty Pharma Limited)
The FDA approved a supplemental application for Ketorolac tromethamine filed by Onesource Specialty Pharma Limited.
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FDA approval · 2016-04-26FDA Approved: XTAMPZA ER — Original Application (Collegium Pharmaceutical, Inc.)
The FDA approved XTAMPZA ER, an extended-release oxycodone product from Collegium Pharmaceutical, for the management of chronic pain in adul…
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FDA approval · 2016-04-20FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (VistaPharm, LLC)
The FDA approved a supplemental application for methadone hydrochloride (ANDA040241) submitted by VistaPharm, LLC.
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FDA approval · 2016-04-20FDA Approved: OXYCONTIN — Supplemental Application (Purdue Pharma LP)
The FDA approved Purdue Pharma LP's supplemental application for OXYCONTIN (oxycodone hydrochloride), updating labeling as part of the suppl…
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FDA approval · 2016-04-20FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (VistaPharm, LLC)
The FDA approved a supplemental application for methadone hydrochloride by VistaPharm, LLC, representing an approved change to an already-ap…
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FDA approval · 2016-04-20FDA Approved: MORPHINE SULFATE EXTENDED RELEASE — Supplemental Application (Rhodes Pharmaceuticals L. P.)
FDA approved a supplemental application for Morphine Sulfate Extended Release submitted by Rhodes Pharmaceuticals L.P.
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FDA approval · 2016-04-20FDA Approved: MORPHINE SULFATE — Supplemental Application (Upsher-Smith Laboratories, LLC)
The FDA granted approval for a supplemental application for Morphine Sulfate, submitted by Upsher-Smith Laboratories, LLC.
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FDA approval · 2016-04-20FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Aurolife Pharma, LLC)
FDA approved Aurolife Pharma's supplemental application for methadone hydrochloride, granting approval of a generic methadone hydrochloride …
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FDA approval · 2016-04-20FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Epic Pharma, LLC)
FDA approved a supplemental application for Methadone hydrochloride by Epic Pharma, LLC.