Pain
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Sign up freeTop drugs studied for this disease
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FDA approval · 2025-12-22FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Genus Lifesciences Inc.)
FDA approved a supplemental application for Hydrocodone Bitartrate and Acetaminophen from Genus Lifesciences Inc., enabling its marketing as…
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FDA approval · 2025-12-22FDA Approved: OXYCODONE AND ACETAMINOPHEN — Supplemental Application (Granules Pharmaceuticals Inc.)
FDA approves Granules Pharmaceuticals Inc.'s supplemental application to market a generic oxycodone/acetaminophen product (ANDA 211708).
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FDA approval · 2025-12-22FDA Approved: PROLATE — Supplemental Application (Forte Bio-Pharma LLC)
FDA approved a supplemental application for PROLATE (oxycodone hydrochloride and acetaminophen) from Forte Bio-Pharma LLC.
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FDA approval · 2025-12-22FDA Approved: BELBUCA — Supplemental Application (BioDelivery Sciences International Inc)
The FDA approved a supplemental application for Belbuca (buprenorphine hydrochloride) from BioDelivery Sciences International Inc.
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FDA approval · 2025-12-22FDA Approved: DISKETS — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approves a supplemental application for DISKETS (methadone hydrochloride) by Hikma Pharmaceuticals USA Inc. The approval expands the lab…
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FDA approval · 2025-12-22FDA Approved: OLINVYK — Supplemental Application (Trevena, Inc.)
The FDA approved a supplemental application for OLINVYK (oliceridine) from Trevena, Inc. This action updates the product labeling as part of…
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FDA approval · 2025-12-22FDA Approved: TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN — Supplemental Application (Micro Labs Limited)
FDA approved a supplemental application for tramadol hydrochloride and acetaminophen from Micro Labs Limited.
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FDA approval · 2025-12-22FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Camber Pharmaceuticals, Inc)
FDA approved a supplemental application for Methadone Hydrochloride from Camber Pharmaceuticals, Inc, updating the product’s regulatory stat…
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FDA approval · 2025-12-22FDA Approved: ACETAMINOPHEN AND CODEINE PHOSPHATE — Supplemental Application (Elite Laboratories, Inc.)
FDA approved a supplemental application for Acetaminophen and Codeine Phosphate from Elite Laboratories, Inc., for its analgesic combination…
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FDA approval · 2025-12-22FDA Approved: BUPRENORPHINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for buprenorphine from Sun Pharmaceutical Industries, Inc.
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FDA approval · 2025-12-22FDA Approved: DSUVIA — Supplemental Application (AcelRx Pharmaceuticals, Inc.)
FDA approved a supplemental application for DSUVIA (sufentanil) by AcelRx Pharmaceuticals, Inc., authorizing changes to the NDA. The approva…
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FDA approval · 2025-12-22FDA Approved: BUTORPHANOL TARTRATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for butorphanol tartrate from Hikma Pharmaceuticals USA Inc., enabling the marketing of a generi…
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FDA approval · 2025-12-22FDA Approved: MORPHINE SULFATE — Supplemental Application (Fresenius Kabi, USA LLC)
FDA approved a supplemental application for Morphine Sulfate submitted by Fresenius Kabi, USA LLC.
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FDA approval · 2025-12-22FDA Approved: LEVORPHANOL TARTRATE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for Levorphanol Tartrate submitted by SpecGx LLC.
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FDA approval · 2025-12-22FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
The FDA approved a supplemental application for hydrocodone bitartrate and acetaminophen from Rhodes Pharmaceuticals L.P., granting approval…
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FDA approval · 2025-12-22FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Epic Pharma, LLC)
FDA approved a supplemental application for methadone hydrochloride (Epic Pharma, LLC), approving a generic product under the ANDA pathway.
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FDA approval · 2025-12-22FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for METHADONE HYDROCHLORIDE from SpecGx LLC, confirming the generic product under ANDA 207537. This …
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FDA approval · 2025-12-22FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc., resulting in a generic product appr…
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FDA approval · 2025-12-22FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for a generic hydrocodone bitartrate and acetaminophen product by SpecGx LLC.
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FDA approval · 2025-12-22FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Elite Laboratories, Inc.)
FDA approved a supplemental application for methadone hydrochloride (generic) from Elite Laboratories, Inc.
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FDA approval · 2025-12-15FDA Approved: TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA granted supplemental approval for Amneal Pharmaceuticals of New York LLC to market tramadol hydrochloride and acetaminophen as a generic…
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FDA approval · 2025-12-15FDA Approved: TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application from Aurobindo Pharma Limited for the tramadol hydrochloride and acetaminophen combination.
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FDA approval · 2025-11-25FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for Amneal's generic hydrocodone bitartrate and acetaminophen, enabling its use as an analgesic for …
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FDA approval · 2025-11-19FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Eywa Pharma Inc)
FDA approved Eywa Pharma Inc's supplemental application for Hydrocodone Bitartrate and Acetaminophen. The approval relates to changes under …
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FDA approval · 2025-10-17FDA Approved: OXYMORPHONE HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
The FDA approved a supplemental application for oxymorphone hydrochloride from Amneal Pharmaceuticals of New York LLC. The action confirms a…