Pain
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Sign up freeTop drugs studied for this disease
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FDA approval · 2020-11-17FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Camber Pharmaceuticals, Inc.)
The FDA approved a supplemental application for Camber Pharmaceuticals' generic hydrocodone bitartrate and acetaminophen tablet, enabling it…
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FDA approval · 2020-11-02FDA Approved: METHADONE HYDROCLORIDE DYE-FREE, SUGAR-FREE, UNFLAVORED — Original Application (Lannett Company, Inc.)
FDA approved Lannett's methadone hydrochloride dye-free, sugar-free, unflavored product through an Original Application (ANDA), adding a new…
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FDA approval · 2020-10-28FDA Approved: ALEVE GELCAPS — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application to add Aleve GelCaps (naproxen sodium) as a new gelcap dosage form for naproxen sodium, expanding th…
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FDA approval · 2020-10-20FDA Approved: KETOROLAC TROMETHAMINE — Original Application (Eugia US LLC)
FDA approves Eugia US LLC's original generic application for ketorolac tromethamine, authorizing its marketing as a non-steroidal anti-infla…
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FDA approval · 2020-09-01FDA Approved: TRAMADOL HYDROCHLORIDE — Original Application (TruPharma, LLC)
FDA approved tramadol hydrochloride under an original application (NDA214044) for TruPharma, LLC.
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FDA approval · 2020-08-20FDA Approved: KETOROLAC TROMETHAMINE — Original Application (Nephron Pharmaceuticals Corporation)
FDA approved an original ANDA for ketorolac tromethamine from Nephron Pharmaceuticals Corporation, granting generic status for this NSAID.
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FDA approval · 2020-06-23FDA Approved: BUPRENORPHINE HYDROCHLORIDE — Supplemental Application (Par Health USA, LLC)
The FDA approved a supplemental application for buprenorphine hydrochloride submitted by Par Health USA, LLC.
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FDA approval · 2020-06-15FDA Approved: BUPRENORPHINE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approves Hikma Pharmaceuticals USA Inc.'s supplemental application for buprenorphine hydrochloride, enabling a generic product entry…
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FDA approval · 2020-05-05FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for methadone hydrochloride manufactured by Hikma Pharmaceuticals USA Inc.
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FDA approval · 2020-04-06FDA Approved: ALEVE PM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Aleve PM, adding the diphenhydramine HCl and naproxen sodium combination (Bayer HealthCare LLC) …
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FDA approval · 2020-03-16FDA Approved: METHADONE HYDROCHLORIDE — Original Application (VistaPharm, LLC)
FDA approves VistaPharm's methadone hydrochloride as a generic drug under an original ANDA; the product is intended for analgesic use and fo…
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FDA approval · 2020-03-06FDA Approved: CELECOXIB — Original Application (Chartwell RX, LLC)
FDA approved the original generic application for celecoxib (Celecoxib) by Chartwell RX, LLC.
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FDA approval · 2020-02-25FDA Approved: CELECOXIB — Original Application (EPIC PHARMA, LLC)
FDA approved the Original Application (ANDA) for a generic Celecoxib product from Epic Pharma, LLC, enabling its marketing as a COX-2 inhibi…
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FDA approval · 2020-01-27FDA Approved: OXYCODONE HYDROCHLORIDE ORAL SOLUTION — Original Application (Aurolife Pharma, LLC)
FDA approved Aurolife Pharma's generic oxycodone hydrochloride oral solution for the management of moderate to severe pain where an opioid a…
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FDA approval · 2020-01-03FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Original Application (Granules Pharmaceuticals Inc.)
The FDA approved Granules Pharmaceuticals' hydrocodone bitartrate and acetaminophen product under an original application.
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FDA approval · 2019-12-03FDA Approved: DICLOFENAC POTASSIUM — Original Application (Lifsa Drugs LLC)
FDA approved the original application for diclofenac potassium as a generic NSAID for relief of pain and inflammation associated with variou…
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FDA approval · 2019-11-27FDA Approved: CELECOXIB — Original Application (NIVAGEN PHARMACEUTICALS, INC.)
The FDA approved NIVAGEN Pharmaceuticals, Inc.'s original application for a generic celecoxib product.
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FDA approval · 2019-10-13FDA Approved: KETOROLAC TROMETHAMINE — Supplemental Application (Sandoz Inc)
FDA approved a supplemental application for ketorolac tromethamine filed by Sandoz Inc under an approved ANDA.
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FDA approval · 2019-10-11FDA Approved: OXYCODONE AND ACETAMINOPHEN — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for a generic oxycodone hydrochloride and acetaminophen product (Oxycodone and Acetaminophen) manufa…
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FDA approval · 2019-10-11FDA Approved: TRAMADOL HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for tramadol hydrochloride submitted by Sun Pharmaceutical Industries, Inc. This action expands/…
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FDA approval · 2019-10-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (PAI Holdings, LLC dba PAI Pharma)
FDA approves a supplemental application for Hydrocodone Bitartrate and Acetaminophen (PAI Pharma), authorizing continued marketing of this a…
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FDA approval · 2019-10-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Lupin Pharmaceuticals,Inc.)
The FDA approved Lupin Pharmaceuticals' supplemental application for hydrocodone bitartrate and acetaminophen. This action adds or updates t…
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FDA approval · 2019-10-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for Hydrocodone Bitartrate and Acetaminophen by SpecGx LLC (ANDA) under a supplemental approval.
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FDA approval · 2019-10-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (KVK-Tech, Inc.)
FDA approved a supplemental application for KVK-Tech's hydrocodone bitartrate and acetaminophen product, authorizing changes under an approv…
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FDA approval · 2019-10-11FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Aurolife Pharma, LLC)
The FDA approved a supplemental application for a generic hydrocodone bitartrate and acetaminophen product by Aurolife Pharma, LLC.